The BD Recykleen™ Sharps Collector is a single use device designed for the safe disposal of regulated medical waste such as contaminated sharps waste. All materials, including sides, bottom, and top are manufactured with polypropylene or polyolefin plastics. The basis of this new Traditional 510(k) submission is for a material change of the sharps collector. The material change, which will incorporate the use of a new resin grade of recycled plastic recovered from the hospital and healthcare facility medical sharps waste-stream. The use of post-hospital recycled resins in the manufacture of the BD Recykleen Sharps Collectors has been demonstrated to be safe and effective. BD has developed the BD ecoFinity™ Life Cycle Solution, which is a program for recycling clinically used hospital-generated medical sharps waste. The basics of this new recycling program are that plastics, recovered from recycling post-hopital sharps waste, are utilized to manufacture new sharps collectors rather than being treated and disposed in landfills or incinerated. After sanitization, the treated sharps waste is separated into metal, light plastics, and other materials. The light plastics are recovered, extruded and pellitized into a final resin pellet form. The recycled resin pellets are then injection molded into components that make up the finished BD Recykleen™ Sharps Collectors.

AI/ML Overview

The provided text describes the BD Recykleen™ Sharps Collector, a single-use device designed for the safe disposal of regulated medical waste. The primary change in this 510(k) submission is the incorporation of a new resin grade of recycled plastic from the hospital and healthcare facility medical sharps waste-stream. The manufacturer, BD Medical Surgical Systems, asserts that the new device is substantially equivalent to the legally marketed BD Guardian™ Sharps Collector (K943134).

Here's a breakdown of the acceptance criteria and study information:

1. Table of Acceptance Criteria and Reported Device Performance

Acceptance Criteria	Test Standard/Method	Pass/Fail Criteria	Reported Device Performance
Puncture Resistance	ASTM F2132-01 (2008), "Standard Specification for Puncture Resistance of Materials Used in Containers for Discarded Medical Needles and Other Sharps".	No single needle puncture force less than 2.8 lbf. Average puncture force of 3.4 lbf.	Met: Individual NPR regression analyses of wall thickness versus needle puncture force were completed for each of the following: 100% recycled resin grades (PH, PI, and PC); virgin and recycled resin blends. Each resin material is characterized to have a unique minimum wall thickness to meet ASTM F 2132-01 (page 6).
Impact Resistance	Drop test (39" from base onto hard surface floor) with a filled collector (assorted sharps/syringes or equivalent weight with resin beads).	No gross fractures (external wall of container open enough to allow escape of solid contents) or loss of contents. Stress fractures permitted.	Met: The results of product performance testing demonstrated equivalent performance to the predicate device performance (page 6).
Leak Resistance	OSHA Specification (29 CFR 1910.1030) - container filled with water to labeled fill line and left to stand for 1 hour.	No leaks observed with product standing in upright position.	Met: The results of product performance testing demonstrated equivalent performance to the predicate device performance (page 6).
Transit Damage Resistance	Shipping case with appropriate number of products dropped from 24" onto a hard surface floor in 10 different orientations.	Product free from any visible damage that may affect customer usage, safety, or satisfaction with a 90% pass rate.	Met: The results of product performance testing demonstrated equivalent performance to the predicate device performance (page 6).
Biocompatibility	ISO 10993 (Cell Toxicity, Murine Local Lymph Node Assay, Primary Dermal Irritation)	Passed	Passed: For both Principle Device (recycled resins) and Predicate Device (virgin PP) (Table 6, page 7).
Bioburden (Resin Pellets)	ISO 11737-1	-	Met: (PI,PC,PH): <46 CFU/10g; Virgin PP: <4.8 CFU/10g (Table 6, page 7).
Bioburden (Sharps Collectors-Interior/Exterior)	-	-	Met: (PI,PC,PH): 1.5 CFU/2 swabs (interior), 10.8 CFU/100mL (exterior); Virgin PP: 3.7 CFU/2 swabs (interior), 3.1 CFU/100mL (exterior) (Table 6, page 7).
Chemical Analysis (Extractibles)	LC/DAD/MS	Same performance as predicate device.	Same: As predicate device (Table 6, page 7).
Chemical Analysis (Leachables)	GC/MS	No significant differences compared to predicate device.	No significant differences: Compared to predicate device (Table 6, page 7).
Heavy Metals	ICP/MS, XRF	Passed, TPCH <100ppm.	Passed: TPCH <100ppm for both principle and predicate devices (Table 6, page 7).

2. Sample Size Used for the Test Set and Data Provenance

The document does not explicitly state the specific number of samples or sample sizes used for each test performed on the BD Recykleen™ Sharps Collector. However, it indicates:

Needle Penetration Resistance: "cutting 12 samples from needle containment areas of the sharps collector" (page 6).
Data Provenance: The new device incorporates recycled plastic recovered from the hospital and healthcare facility medical sharps waste-stream (page 1). Testing was performed to demonstrate substantial equivalence to existing BD Sharps Collectors. The data is prospective, generated specifically for this 510(k) submission to demonstrate the performance of the new design. The country of origin for the data is not specified but is implicitly in line with U.S. regulatory standards (ASTM, OSHA, ISO).

3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications of Those Experts

This type of information (number and qualifications of experts for ground truth) is not applicable to this device and its testing. The device is a physical product (sharps collector), and its performance is evaluated through objective physical and chemical bench testing against established standards (e.g., ASTM, OSHA, ISO), not through expert interpretation or clinical assessment that would require ground truth established by medical experts.

4. Adjudication Method for the Test Set

Again, an adjudication method (like 2+1, 3+1 consensus) is not applicable to the testing for this device. The testing is based on objective, measurable physical and chemical properties and predefined pass/fail criteria, not on subjective assessments requiring expert consensus.

5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study Was Done

No, a Multi-Reader Multi-Case (MRMC) comparative effectiveness study was not done. This type of study is relevant for diagnostic devices or AI algorithms that involve human interpretation of medical images or data. The BD Recykleen™ Sharps Collector is a physical medical waste containment device, and its safety and effectiveness are assessed through bench testing, not through human reader studies. Therefore, there is no effect size of human readers improving with or without AI assistance.

6. If a Standalone (i.e., algorithm only without human-in-the-loop performance) Was Done

No, a standalone (algorithm only) performance study was not done. This type of study is also specific to AI/software as a medical device (SaMD). The BD Recykleen™ Sharps Collector is a physical device, and its performance is evaluated through bench testing.

7. The Type of Ground Truth Used

The "ground truth" for the performance of the BD Recykleen™ Sharps Collector is established by objective performance standards and specifications. These include:

ASTM F2132-01 (Reapproved 2008) e1: "Standard Specification for Puncture Resistance of Materials Used in Collectors for Discarded Medical Needles and Other Sharps."
OSHA Regulation 29 CFR Part 1910.1030: Relevant for leak resistance.
ISO 10993: For Biocompatibility testing.
ISO 11737-1: For Bioburden testing.
Internal BD specifications: For tests like Impact Resistance and Transit Damage Resistance, which have clearly defined pass/fail criteria.
Chemical Analysis Methods: LC/DAD/MS, GC/MS, ICP/MS, XRF to assess material composition and potential contaminants.

These standards and methods define what constitutes acceptable performance for a sharps collector, serving as the objective ground truth against which the device's actual performance is measured.

8. The Sample Size for the Training Set

Not applicable. The BD Recykleen™ Sharps Collector is a physical medical device, not an AI algorithm or diagnostic tool. Therefore, a "training set" in the context of machine learning is not relevant here. The manufacturing process and material properties are developed and validated through engineering design, material science, and performance testing, not through iterative training on a dataset.

9. How the Ground Truth for the Training Set Was Established

Not applicable, as there is no "training set" in the context of this device. The physical and chemical properties of the materials and the design of the device are developed and verified through established engineering and materials science principles, and tested against recognized industry and regulatory standards.

Summary

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MAR 2 8 2012

K112774 510k SUMMARY BD Recykleen™ Sharps Collector

Date: March 28, 2012

Submitted By

BD Medical Surgical Systems Becton, Dickinson and Company 1 Becton Drive Franklin Lakes, New Jersey, 07417 USA

2. Contact Information

Primary Contact Eileen Hiller Director, Regulatory Affairs BD Medical Surgical Systems 1 Becton Drive Franklin Lakes. New Jersey 07417 USA 201-847-4570 Eileen Hiller@BD.com

Secondary Contact

Sergio Gadaleta Vice President, Regulatory Affairs BD Medical Surgical Systems 1 Becton Drive Franklin Lakes, New Jersey 07417 USA 201-847-4496 Sergio Gadaleta@BD.com

3 .- Device identification :-
-Trade Name:	BD-Rec
Common Name:	Sharps
Classification:	MMK -
	needles
Allian William Harris, College, Comment	And Antiques and the manufacturer of the contribution of the contribution of the

CFR Reference: Classification Panel:

cykleen TM-Sharps Container-Container Accessory to hypodermic single lumen 21CFR 880.5570 - Class II General Hospital

4. Predicate devices:

Substantial equivalence is being claimed to the following legally marketed devices:

Trade Name: BD Guardian™ Sharps Collector Common Name: Sharps Container Classification: MMK - Accessory to hypodermic single lumen needles Predicate 510k No K943134 Cleared 11/07/1994 21CFR 880.5570 - Class II CFR Reference:

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Classification Panel:

General Hospital

5. Product Description:

The basis of this new Traditional 510(k) submission is for a material change of the sharps collector. The material change, which will incorporate the use of a new resin grade of recycled plastic recovered from the hospital and healthcare facility medical sharps waste-stream. The use of post-hospital recycled resins in the manufacture of the BD Recykleen Sharps Collectors has been demonstrated to be safe and effective. BD has developed the BD ecoFinity™ Life Cycle Solution, which is a program for recycling clinically used hospital-generated medical sharps waste. The basics of this new recycling program are that plastics, recovered from recycling post-hopital sharps waste, are utilized to manufacture new sharps collectors rather than being treated and disposed in landfills or incinerated. After sanitization, the treated sharps waste is separated into metal, light plastics, and other materials. The light plastics are recovered, extruded and pellitized into a final resin pellet form. The recycled resin pellets are then injection molded into components that make up the finished BD Recykleen™ Sharps Collectors.

The technological and performance characterisitics of the BD Recykleen™ Sharps-Collectors (new-device) is similar-to-BD-Guardian Sharps-Collectors. (predicate device). There is no change to the intended use of the new or predicate Sharps Collectors, the collector design and technological and performance characteristics remain unchanged.

BD Sharps Collectors may be used with optional accessories, stabilizer and brackets, that provide the customer choices for further security and enhanced stability during usage. The 8Qt and 6 Gallon Product Instructions for Use list the compatible brackets and stabilizer accessories available.

Brackets are designed to secure the collector to a wall or cart. Some bracket accessories include additional security via a locking mechanism.

Stabilizers: Stabilizers are designed to stabilize collectors on a countertop or other flat surface.

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6. Intended Use:

The BD Recykleen™ Sharps Collectors intended use:

Sharps Collectors are intended to be used for disposal of contaminated medical sharps in health care facilities

7. Comparison to Predicate Devices:

The sharps container is similar to the predicated in intended use, materials, measuring principle and performance.

FEATURE	MODIFIED DEVICEBD RECYKLEENTMSHARPS COLLECTOR	PREDICATE DEVICEBD GUARDIANTM SHARPSCOLLECTOR
Closable	Same	Yes, Snap fit cap/closure
Puncture Resistant	SameASTM F2132-01 (2008),"Standard Specification forPuncture Resistance ofMaterials Used in Containersfor Discarded MedicalNeedles and Other Sharps".	Yes Passes proposed ASTMF04.65.01 procedure(Current draft in 1994)
Leakproof on sidesandBottom	Same	Yes
Labeled or Color-Coded:	Same	Sharps/Infectious WasteYes
Biohazard WarningLabel
Fluorescent orangeor orange-red withlettering incontrasting color	Same	Yes
Affixed to container	Same	Yes
Red Container orlabel	Same	Yes
Recycled ContentLabel	Patient Room CollectorsRecycled Content- Minimum20%Nestable CollectorsMinimum 50% RecycledContent	NA
FEATURE	MODIFIED DEVICEBD RECYKLEENTMSHARPS COLLECTOR	PREDICATE DEVICEBD GUARDIANTM SHARPSCOLLECTOR
Capable ofmaintaining stable,upright position.	Same	Yes
No feature to bend,break, or shearneedle.	Same	No feature present.
Unwinder	Same	Unwinder is designed for one-handed operation on containers.Labeling is "Single Use Only"
Reusable SharpContainer	Same
Overfill Indication	Same	"Do Not Overfill" or "Fill to thisLevel Only" is labeled orembossed on container at thelocation of overfill. Labelingincludes a "Fill Line."
Locking Enclosure	Same	All models have the option foruse of security locks and keys
Holder to secure towalls	Same	Product is capable of attaching towall-mount or cart-mount.
Materials	Polyolefinic resins:Virgin polypropylenePost consumerPost industrialPost hospital	Polyolefinic resins- VirginPolypropylene
Construction	Same	Injection molded Container,Injection molded Lids/Closures
Clarity	Same	Each Collector has a minimumof one translucent component,either base or top. Some modelswith clear "see thru" tops.
Recycled Content	Nestable Sharps Collectorsminimum 50%	N/A

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The Device Models Subject to this submission are listed below. The BD Recykleen™ Sharps collector's dimensions, access openings, features and capacity are essentially equivalent to the predicate devices.

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Family	BDRecykleen™SharpsCollector	Access Openingand Closure	AccessOpeningSize	Length (in)	Width(in)	Height(in)	Weight(grams)	Capacity
NestableSharpsCollectors	8 QuartModel No. 305059	Funnel Top, withrestricted accesspetalsHinge Cap	1.5 "x1.125"withflexiblepetals	9.75	10.00	6.75	446	8 Quarts
	6 GallonModel No. 305160	Open top withrestricted accessopeningHinge Cap	2.5"diameter	17.50	12.50	8.50	935	6 Gallons

8. Discussion of Similarities and Differences in New and Predicate Product

Intended Use Comparison

The indications for use of the new BD Recykleen™ Sharps Collector are not new indications in that they are the same as those for the predicated devices. Sharps collectors-and-other-predicated-devices-are-containers-intended-for-the-disposal-ofcontaminated medical waste within healthcare facilities.

\ Design and Materials Comparison

The design and functionality of the sharps collectors and predicated devices are identical. They are constructed from polypropylene and contain a component(s) made from recycled polyolefin plastics and are intended for single use only. All of the devices conform to recognized standard, ASTM F-2132-01 for needle penetration resistance. They have features to prevent contact between user and the contents, and are designed for easy and safe determination of fullness. None of the devices have features that bend, break, or shear needles.

9. Summary of Performance Bench Testing of Device Modifications

9.1 Performance Standards:

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No performance standards have been established under Section 514 for this product code. All recognized standards and other regulations and guidance documents that were used in this 510(k) have been listed in Section 20.

The performance testing demonstrates compliance with the recognized consensus standard, ASTM F 2132-01 (Reapproved 2008) e1, "Standard Specification for Puncture Resistance of Materials Used in Collectors for Discarded Medical Needles and Other Sharps." In addition the relevant FDA guidance document, "Guidance on the Content and Format of Premarket Notification [510(K)] Submission for Sharps Collectors" dated October 1993, was used to identify applicable physical and mechanical features of the modified and predicate devices.

All applicable standards have been used to show that the BD Recykleen Container family is substantially equivalent to the appropriately listed predicate devices.

The performance testing summary demonstrates substantial equivalence between the modified device and the predicate devices. The new sharps collectors have been tested by appropriate methods with respect to relevant FDA guidance documents, FDA recognized ASTM standards F 2132-01 and OSHA regulations 29 CFR Part 1910:1030. No new issues of safety and effectiveness were raised with the testing performed, and the BD Recykleen Containers are considered substantially equivalent to its predicate device.

Performance Testing (Bench) -Product Testing 9.2

The BD Recykleen™ Sharps Containers incorporate the identical collector design features, performance characteristics, manufacturing technology. The results of product_performance_testing_demonstrated_equivalent_performance_to_predicate_device performance and no new issues of concern-were raised.

Impact Resistance

ﺔ ﻣﻤﺜﻠ

Impact resistance was assessed such that no open fractures or disassembly results when a filled collector is dropped. The container is filled with assorted sharps or syringes with or without needles, or equivalent weight using resin beads and sealed as if ready for transport. The collector is dropped 39" from the base onto a hard surface floor.

Pass/Fail Criteria: No gross fractures (external wall of container is open enough to allow escape of solid contents) or loss of contents are permitted. Stress fractures (crack in external wall where wall does not separate to release solid contents) are permitted.

Needle Penetration Resistance

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Needle Penetration Resistance is based on ASTM F2132-01, "Standard Specification for Puncture Resistance of Materials Used in Containers for Discarded Medical Needles and Other Sharps". for minimum and average needle penetration force. The test method involves cutting 12 samples from needle containment areas of the sharps collector. Each sample is tested using a motorized mechanical tester (Instron, ATS or equivalent) with a new 21 gauge x 1" needle, each penetration is tested at 4"/minute.

Pass/Fail Criteria: No one needle puncture force can be less than 2.8 lbf and average puncture force of 3.4 lbf must be met to be acceptable.

Leak Resistance

The Leak Resistance testing is based on OSHA Specification (29 CFR 1910.1030) -The container is filled with water to the labeled fill line and left to stand on its base 1 hour.

Pass/Fail Criteria: No leaks are observed with product standing in upright position.

Transit Damage Resistance:

Transit Damage testing demonstrates the product is free from any visible damage that may affect customer usage, safety, or satisfaction when products are packaged in shipping cases and dropped. The appropriate number of products are packaged in the appropriate shipping case and sealed as if ready for shipment. The shipping case is dropped from 24" onto a hard surface floor in 10 different orientations.

Pass/Fail Criteria: The product is free from any visible damage that may affect customer usage, safety, or satisfaction when products are packaged in the shipping case and dropped with a 90% pass rate.

Performance Testing- Needle Penetration Resistance- Comparison of all Recycled Resin Grades and blend of resins in use

The critical performance characteristic for Sharps Collectors is Needle Penetration Resistance (NPR). Individual NPR regression analyses of wall thickness versus needle puncture force were completed for each of the following: 100% recycled resin grades (PH, PI, and PC); virgin and recycled resin blends. The NPR regression curves were completed for each virgin material, recycled resin blend formulation. Each resin material is characterized to have a unique minimum wall thickness to meet ASTM F 2132-01.

ਰੇ ਤੇ Safety Tests

To demonstrate that post hospital recycled resins are substantially equivalent to the PC and PI recycled resins and virgin resins used in the predicate Sharps Collectors. additional safety tests were conducted. These tests were selected to eliminate

BD Recykleen Sharps Collector 510k Summary

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potential concerns of residual resin contamination after completion of the sanitization, separation, recycling and extrusion processes.

Pellet samples or test plaques representing 100% PH, 100% PI, and 100% PC recycled and virgin resins were tested according to those listed in Table 6.

All Safety Tests demonstrated equivalent performance between the principle and predicate Sharps Collectors and individual resins tests.

Safety Test	Standards/Method	Principle Device	Predicate Device
Biocompatibility TestingCell Toxicity Murine Local Lymph Node Assay Primary Dermal Irritation	ISO 10993ISO 10993ISO 10993	passedpassedpassed	passedpassedpassed
Bioburden-All test samples- non sterile SamplesResinPellets	ISO 11737-1	(PI,PC,PH)	Virgin PP
Sharps CollectorsInterior exterior		<46 CFU/10g1.5 CFU/2 swabs10.8 CFU/100mL	<4.8 CFU/10g3.7 CFU/2 swabs3.1 CFU/100mL
Chemical AnalysisExtractible: liquid extracts (water/alcohol)	LC/DAD/MS	Same	Same
Leachable:volatiles/headspace	GC/MS	No significant differences	No significant differences
Heavy Metals	ICP/MSXRF	PassedTPCH<100ppm	PassedTCPH<100ppm

Table 6 Summary of Safety Tests

Conclusion:

BD Recykleen™ Sharps Collectors proves to be substantially equivalent to the respective predicate sharps collectors.

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DEPARTMENT OF HEALTH & HUMAN SERVICES

Image /page/8/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with its wings spread, symbolizing protection and care. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" are arranged in a circular pattern around the eagle, indicating the department's name and national affiliation. The logo is simple, using only black and white, which gives it a clean and official appearance.

Public Health Service

Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002

Ms. Eileen Hiller Manager of Regulatory Affairs Becton, Dickinson and Company BD Medical Surgical 1 Becton Drive MC 237 Franklin Lakes, New Jersey 07417

MAR 2 8 2012

Re: K112774

Trade/Device Name: BD Recykleen" Nestable Sharps Collectors Regulation Number: 21 CFR 880.5570 Regulation Name: Hypodermic Single Lumen Needle Regulatory Class: II Product Code: MMK Dated: March 20, 2012 Received: March 22, 2012

Dear Ms. Hiller:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

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Page 2 - Ms. Hiller

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices /ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.

Sincerely yours,

Anthony D. Watson, B.S., M.S., M.B.A. Director

Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation · Center for Devices and Radiological Health

Enclosure

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Indications for Use Statement

510(k) Number (if known):

K112774

Device Name:

BD Recykleen™ Nestable Sharps Collectors

Model Number Size

305059 8 Quart Nestable Sharps Collector

Model Number Size

305160 6 Gallon Nestable Sharps Collector

Indications for Use:

Sharps collectors are intended to be used for the disposal of contaminated medical sharps in health care facilities.

Prescription Use (Part 21 CFR 801 Subpart D)

Over-The-Counter Use AND/OR X (21 CFR 801 Subpart C)

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Elizabeth B. (Lamie-Wells

(Division Sign-Uff) Division of Anesthesiology, General Hospital Infection Control, Dental Devices

510(k) Number:

Confidential & Proprietary

0000006

Regulation Number and Section

§ 880.5570 Hypodermic single lumen needle.

(a)
Identification. A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.(b)
Classification. Class II (performance standards).