FDA 510(k)

VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER

K-Number: K943138 · 1994-11-28

Decision Date1994-11-28

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Med-Safe Systems, Inc.. It received FDA 510(k) clearance on 1994-11-28 under 510(k) number K943138. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER?

VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is Med-Safe Systems, Inc.. The 510(k) number is K943138.

When did VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER receive FDA 510(k) clearance?

VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER received FDA 510(k) clearance on 1994-11-28, under 510(k) number K943138.

Who is the listed applicant for VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER?

The FDA 510(k) record lists Med-Safe Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER?

The FDA product code for VACUTAINER BRAND NEEDLE DISPOSAL CONTAINER is MMK.

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Other records listing Med-Safe Systems, Inc. as applicant

K943139B-D GUARDIAN ONE PIECE SHARPS COLLECTORS K943135MED-SAFE INSULIN SHARPS CONTAINER K943134B-D GUARDIAN NESTABLE SHARPS COLLECTORS K943141B-D GUARDIAN POINT OF USE HORIZONTAL AND SIDE ENTRY SHARPS COLLECTORS K943137B-D/BFI MAIL DISPOSAL SERVICE K943140B-D GURADIAN CHEMOTHERAPY SHARPS COLLECTORS

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Related Devices (Code: MMK)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.