(294 days)
Not Found
No
The device description details a purely mechanical syringe with a retraction mechanism. There is no mention of software, data processing, or any computational elements that would suggest the use of AI or ML.
No
The device is a syringe used for injecting or withdrawing fluids, and its primary therapeutic function is to safely administer or remove substances from the body, rather than directly treating a condition itself. The safety features are to prevent injury and reuse, not to provide therapy.
No
Explanation: The device is a safety syringe used for injecting or withdrawing fluids, with features to prevent needle stick injuries and syringe reuse; it does not perform diagnostic functions.
No
The device description clearly outlines multiple physical components (barrel, plunger, needle, etc.) and its function involves mechanical actions (injection, withdrawal, retraction). There is no mention of software as a component or function.
Based on the provided information, the Medline Retractable Safety Syringe is not an In Vitro Diagnostic (IVD) device.
Here's why:
- Intended Use: The intended use is clearly stated as "to inject fluids into, or withdraw fluids from, the body." This describes a direct interaction with the patient's body for therapeutic or diagnostic purposes within the body, not for testing samples outside the body.
- Device Description: The description details the mechanical components of a syringe designed for fluid delivery and withdrawal, with a safety mechanism for needle retraction. There is no mention of components or functions related to analyzing biological samples.
- Lack of IVD Characteristics: The document does not mention any of the typical characteristics of an IVD, such as:
- Testing of biological samples (blood, urine, tissue, etc.)
- Reagents or assays
- Measurement of analytes
- Diagnostic information derived from sample analysis
In summary, the Medline Retractable Safety Syringe is a medical device used for administering or collecting substances directly from a patient, which falls under the category of devices used in vivo, not in vitro.
N/A
Intended Use / Indications for Use
The intended use of this device is to inject fluids into, or withdraw fluids from, the body. In addition, this retractable safety syringe is designed to aid in the prevention of needle stick injuries and reduce the potential for syringe reuse.
Product codes (comma separated list FDA assigned to the subject device)
MEG
Device Description
The Medline Retractable Safety Syringe is a retractable type piston syringe, designed to aid in the prevention of needle stick injuries. This single-use, disposable syringe consists of the following components:
-
Barrel - The barrel has a scale showing the capacity of the syringe. In addition, the tip of the barrel has a luer lock fitting for the user in affach a needle. As a strenger and
-
Plunger - Once the plunger is fully depressed, it engages the needle assembly. As the plunger is retracted, the needle assembly is retracted into the barrel. Once the plunger is fully retracted and locked in place, the plunger is snapped off leaving the needle in the barrel of the syringe.
-
O-Ring - The O-ring minimizes the risk of leakage around the adapter.
-
Gasket - The gasket maintains the fluid in the barrel between the adapter and plunger.
-
Luer Lock or Needle Holder - The luer lock facilitates passage of the fluid, while holding the needle in place.
-
Hub Holder - Engages the plunger after the injection.
-
Locking Ring - A plastic insert at the top of the barrel. After the injection, the health care professional retracts the plunger with the needle into the barrel. Once the plunger is fully retracted, the plunger is locked into position at the top of the barrel. This safety mechanism makes sure the needle cannot be pushed back out the tip of the barrel.
-
Needle - Pre-attached single lumen stainless steel needle which penetrates the patient's skin to inject/withdraw fluid. (1ml syringe only)
-
Short Cap - Protective cover for the needle tip. Removed upon use. (1ml syringe only)
-
Big Cap - Protective cover for the plunger. (1ml syringe only)
The Medline Retractable Safety Syringe functions in a manner similar to standard syringes for fluid injection/withdrawal. After use, the health care professional fully depresses the plunger to engage the luer assembly. Once the luer assembly is engaged, pulling back the plunger causes the adapter and the attached needle to be withdrawn into the safety of the barrel. This retraction into the barrel of the syringe can be visually confirmed. In this position against the flange, single-handed lateral pressure on the plunger results in a controlled fracture of the plunger. Once this safety mechanism has been activated, the syringe is permanently disabled and the needle is completely secured within the barrel. Both the syringe and plunger are discarded in a Sharp's container.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Testing consisted of compliance to the applicable sections of the following testing
- ISO 7886-1:1993 .
- ISO 7886-4:2006 .
- ISO 9626 .
- ISO 594 .
- . ISO 10993
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 880.5860 Piston syringe.
(a)
Identification. A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.(b)
Classification. Class II (performance standards).
0
510(k) Summary
KIOISGO
Submitter Information
Medline Industries, Inc. One Medline Place Mundelein, IL 60060 Contact Person: Matt Clausen Phone Number: 847-643-4785 Date: March 15, 2011
Device Information
Classification Name: Syringe, Antistick Proprietary Name: Medline Retractable Safety Syringe Common Name: Piston or Safety Syringe
Predicate Information
Predicate Name: Inviro Snap Safety Syringe / InviroSnap Safety Syringe Predicate 510(k) #: K032780 / K092430 Predicate Product Code: MEG
Device Description
The Medline Retractable Safety Syringe is a retractable type piston syringe, designed to aid in the prevention of needle stick injuries. This single-use, disposable syringe consists of the following components:
-
Barrel - The barrel has a scale showing the capacity of the syringe. In addition, the tip of the barrel has a luer lock fitting for the user in affach a needle. As a strenger and
-
Plunger - Once the plunger is fully depressed, it engages the needle assembly. As the plunger is retracted, the needle assembly is retracted into the barrel. Once the plunger is fully retracted and locked in place, the plunger is snapped off leaving the needle in the barrel of the syringe.
-
O-Ring - The O-ring minimizes the risk of leakage around the adapter.
-
Gasket - The gasket maintains the fluid in the barrel between the adapter and plunger.
-
Luer Lock or Needle Holder - The luer lock facilitates passage of the fluid, while holding the needle in place.
-
Hub Holder - Engages the plunger after the injection.
-
Locking Ring - A plastic insert at the top of the barrel. After the injection, the health care professional retracts the plunger with the needle into the barrel. Once the plunger is fully retracted, the plunger is locked into position at the top of the barrel. This safety mechanism makes sure the needle cannot be pushed back out the tip of the barrel.
MAR 2 5 2011
1
-
Needle - Pre-attached single lumen stainless steel needle which penetrates the patient's skin to inject/withdraw fluid. (1ml syringe only)
-
Short Cap - Protective cover for the needle tip. Removed upon use. (1ml syringe only)
-
Big Cap - Protective cover for the plunger. (1ml syringe only)
The Medline Retractable Safety Syringe functions in a manner similar to standard syringes for fluid injection/withdrawal. After use, the health care professional fully depresses the plunger to engage the luer assembly. Once the luer assembly is engaged, pulling back the plunger causes the adapter and the attached needle to be withdrawn into the safety of the barrel. This retraction into the barrel of the syringe can be visually confirmed. In this position against the flange, single-handed lateral pressure on the plunger results in a controlled fracture of the plunger. Once this safety mechanism has been activated, the syringe is permanently disabled and the needle is completely secured within the barrel. Both the syringe and plunger are discarded in a Sharp's container.
Indications For Use Statement
The intended use of this device is to inject fluids into, or withdraw fluids from, the body. In addition, this retractable safety syringe is designed to aid in the prevention of needle stick injuries and reduce the potential for syringe reuse.
Comparison of Required Technological Characteristics
Information was submitted to demonstrate that there are no significant differences in technological characteristics between Medline's Retractable Safety Syringe and the cited predicate devices.
Summary and Conclusion of Testing
Testing consisted of compliance to the applicable sections of the following testing
- ISO 7886-1:1993 .
- ISO 7886-4:2006 .
- ISO 9626 .
- ISO 594 .
- . ISO 10993
Conclusion
storidards .
In accordance with 21 CFR Part 807, and based on the information provided in this premarket notification, Medline Industries, Inc. concludes that Medline's Retractable Safety Syringe is safe, effective and substantially equivalent as described herein.
2
Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three stripes representing the department's mission. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged in a circular fashion around the eagle symbol. The logo is in black and white.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
Mr. Matt Clausen Regulatory Affairs Medline Industries, Incorporated One Medline Place Mundelein, Illinois 60060
MAR 2 5 2011
Re: K101560
Trade/Device Name: Medline Retractable Safety Syringe Regulation Number: 21 CFR 880.5860 Regulation Name: Piston Syringe Regulatory Class: II Product Code: MEG Dated: March 7, 2011 Received: March 8, 2011
Dear Mr. Clausen:
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.
3
Page 2- Mr. Clausen
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 clectronic 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
fors 2
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
4
Indications for Use
510(k) Number (if known): K101560
Device Name:
Medline Retractable Safety Syringe
Indications For Use:
The Medline Retractable Safety Syringe is used to inject fluids into, or withdraw fluids from, the body. In addition, this safety syringe is designed to aid in the prevention of needle stick injuries and reduce the potential for syringe reuse.
Prescription Use X (Part 21 CFR 801 Subpart D) OR
Over-the-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of DRH, Office of Device Evaluation (ODE)
(Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices
510(k) Number: K101560