K Number
K955514
Manufacturer
Date Cleared
1996-08-01

(241 days)

Product Code
Regulation Number
880.5570
Reference & Predicate Devices
Predicate For
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

Sharps Safes are designed to be used by Paramedics or Home Care Providers who need a small, portable and rugged sharps container which can be used in remote locations to dispose of contaminated needles.

Device Description

The device is comprised of a 1.5 inch diameter plastic tube (model 1.5), or a 2.0 diameter plastic tube (model 2.0). Securely attached to each end is a plastic cap. Secured inside the cap attached to the bottom end is a hard plastic disc designed to prevent needle penetration. The cap on the top end has a ¼ inch hole in the center. Radiating from the hole are slits cut in the plastic which form flaps through which a sharps can be inserted. A vinyl cover is provided for the top to provide a moisture tight seal.

AI/ML Overview

This document is a 510(k) summary for the DURA-VAC Sharps Safe 1.5 and Sharps Safe 2.0. It describes the device, its intended use, and non-clinical tests. Clinical tests were explicitly stated as "Not required."

Here's the breakdown of the acceptance criteria and the "study" (non-clinical tests) that proves the device meets them:

1. A table of acceptance criteria and the reported device performance

Acceptance Criteria (Implicit)Reported Device Performance (Non-Clinical Tests)
No needle ejection upon impact / Impact ResistanceNo needle ejection when dropped from eight (8) feet onto concrete. No damage to container.
Puncture Resistance (Sides - 1.5")5.12 lb. average for sides.
Puncture Resistance (Bottom - 1.5")6.56 lb. average for bottom.
Puncture Resistance (Sides - 2.0")5.80 lb average for sides.
Puncture Resistance (Bottom - 2.0")6.99 lb. average for bottom.
Wall Thickness (Sides - 1.5").072 inches average for sides.
Wall Thickness (Bottom - 1.5").1174 inches average for bottom.
Wall Thickness (Sides - 2.0").078 inches average for sides.
Wall Thickness (Bottom - 2.0").1125 inches average for bottom.
Sharps Closure Pull Test45 lb. for 24 hours.
Capacity (1.5")15.8 cu. in./6.75 oz.
Capacity (2.0")28.2 cu. in./12.30 oz.
Leakproof (Bottom)The bottom is leakproof.
Leakproof (Top with cover)The top is also leakproof when the vinyl cover is in place.
Disposal (Heavy metals)Sharps Safes contain no heavy metals and can be incinerated.
Attachment Strap StrengthA Sharps Safe will support 45 pounds when secured to a surface by the attachment straps.

2. Sample sized used for the test set and the data provenance

The document does not explicitly state the sample sizes for each non-clinical test performed (e.g., how many units were dropped for impact resistance, or how many tests were done for puncture resistance). It reports average values, implying multiple measurements were taken, but the exact number is missing.

The data provenance is from DURA-VAC, a US-based company (Ventura, CA). The tests are internal non-clinical tests performed by the manufacturer, not external data. The document does not specify if the tests were performed retrospectively or prospectively, but given they are part of a 510(k) submission, they would have been performed prospectively to support the submission.

3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts

This information is not applicable as there was no "ground truth" in the typical sense of expert review for image/data interpretation. The tests were physical and mechanical objective measurements.

However, it is mentioned that "The combined talents of sixty (60) fire department Paramedics were used to develop Sharps Safes." While not establishing "ground truth" for a test set, these paramedics presumably provided input on the practical needs and shortcomings of existing devices, influencing the design and implicit acceptance criteria. Their qualifications are stated as "fire department Paramedics."

4. Adjudication method for the test set

This is not applicable. The non-clinical tests involved objective physical measurements (e.g., weight, distance, force) rather than subjective assessments requiring adjudication.

5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done

No, an MRMC comparative effectiveness study was not done. The document explicitly states "Clinical Tests: Not required." The study focused on the physical and mechanical performance of the device.

6. If a standalone (i.e. algorithm only without human-in-the loop performance) was done

This is not applicable. The device is a physical sharps container, not an algorithm or software. It does not have "standalone" (algorithm-only) performance in the conventional sense of AI/software.

7. The type of ground truth used

For the non-clinical tests described, the "ground truth" was established by objective physical measurements and engineering standards. For example, impact resistance was measured by observation of needle ejection and damage after dropping from a specified height. Puncture resistance was measured by applying force until penetration.

8. The sample size for the training set

This is not applicable. The device is a physical product, not a machine learning model. Therefore, there is no "training set" in the context of data for an algorithm.

9. How the ground truth for the training set was established

This is not applicable as there is no training set for a physical device.

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Image /page/0/Picture/0 description: The image shows a logo for "DURA-VAC" with a caduceus symbol to the left of the text. Below the text is a drawing of a medical equipment case. The address "4464 McGrath STREET" is to the right of the case. The logo appears to be for a medical equipment or supply company.

4464 McGRATH STREET #114 • VENTURA, CA 93003 • (805) 658-7768

AUG - 1 1996

REVISION OF 510K SUMMARY (as required by 807.92 (c)) May 20, 1996

K955514

Submitted by: Neal Shults (owner) 4464 McGrath Street #114 Ventura, CA 93003 (805) 658-7768 (805) 658-8353 (FAX) November 27, 1995

Trade name - Sharps Safe 1.5 Sharps Safe 2.0 Common name - Sharps Container Classification name - Sharps Container 80MMK 880.5570

Equivalent device being legally marketed: Trade name - Sharps A Gator Manufactured by: Devon Industries, Inc. 510K Approval Number: K943892

Description :

The device is comprised of a 1.5 inch diameter plastic tube (model 1.5), or a 2.0 diameter plastic tube (model 2.0). Securely attached to each end is a plastic cap. Secured inside the cap attached to the bottom end is a hard plastic disc designed to prevent needle penetration. The cap on the top end has a ¼ inch hole in the center. Radiating from the hole are slits cut in the plastic which form flaps through which a sharps can be inserted. A vinyl cover is provided for the top to provide a moisture tight seal.

Intended Use :

Sharps Safes are designed to be used by Paramedics or Home Care Providers who need a small, portable and rugged sharps container which can be used in remote locations to dispose of contaminated needles.

Technological Characteristics:

Predicate devices which we surveyed all had some They were either too large, too small, shortcomings. wouldn't contain the sharps if mishandled, blood could leak out,would shatter if struck, couldn't be attached to the outside of a drug box, or the contents couldn't be seen.

All of these failings were addressed when designing the Sharps Safe and eliminated.

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K955514

Image /page/1/Picture/1 description: The image shows the logo for DURA-VAC, which includes a caduceus symbol, the text "DURA-VAC" in bold font, and a line drawing of a rectangular device. Below the logo is the address "4464 McGrath STREET". The logo appears to be for a medical or healthcare-related product or service, given the presence of the caduceus symbol.

4464 McGRATH STREET #114 • VENTURA, CA 93003 • (805) 658-7768

Non Clinical Tests: The summary data derived from mechanical testing are as follows : No needle ejection when dropped l)Impact Resistance: from eight (8) feet onto concrete. No damage to container. 2)Puncture Resistance: 1.5 - 5.12 lb. average for sides. 6.56 lb. average for bottom. 2.0 - 5.80 lb average for sides. 6.99 lb. average for bottom. 3)Wall Thickness: l.5 - .072 inches average for sides. .1174 inches average for bottom. 2.0 -.078 inches average for sides. .1125 inches average for bottom. 4)Sharps Closure - Pull Test - 45 lb. for 24 hours. 5)Capacity: 1.5 - 15.8 cu. in./6.75 oz. 2.0 - 28.2 cu. in./12.30 oz. 6)Leakproof Test: The bottom is leakproof. The top is also leakproof when the vinyl cover is in place. 7)Disposal: Sharps Safes contain no heavy metals and can be incinerated. 8)Attachment Strap Test: A Sharps Safe will support 45 pounds when secured to a surface by the attachment straps .

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K45514

Image /page/2/Picture/1 description: The image shows the logo for DURA-VAC, which is written in bold, black letters. To the left of the company name is a medical symbol. Below the company name is the address, 4464 McGrath Street, and an image of a piece of equipment.

4464 MeGRATH STREET #114 • VENTURA, CA 93003 • (805) 658-7768

Clinical Tests :

Not required.

Conclusions :

It is very clear that there is a real need for a sharps container that is designed specifically for Paramedics and Home Health Care Professionals.

All of the existing devices on the market have shortcomings which make them unsuitable for Paramedic use. Sharps Safes were designed to fill this void.

The nonclinical tests provided us with the design and materials to be used, and the clinical tests refined the parameters of the materials. These tests also revealed that a better system was needed to secure the container to the drug box. It also became apparent that two sizes would be beneficial (2 inch and l.5 inch).

The combined talents of sixty (60) fire department Paramedics were used to develop Sharps Safes.

We feel that they meet the need.

§ 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).