FDA 510(k)

POINT OF USE SHARPS A GATOR

K-Number: K943892 · 1994-12-02

Decision Date1994-12-02

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

POINT OF USE SHARPS A GATOR is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1994-12-02 under 510(k) number K943892. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POINT OF USE SHARPS A GATOR?

POINT OF USE SHARPS A GATOR is a medical device that received FDA 510(k) clearance on 1994-12-02. The listed applicant is Devon Industries, Inc.. The 510(k) number is K943892.

When did POINT OF USE SHARPS A GATOR receive FDA 510(k) clearance?

POINT OF USE SHARPS A GATOR received FDA 510(k) clearance on 1994-12-02, under 510(k) number K943892.

Who is the listed applicant for POINT OF USE SHARPS A GATOR?

The FDA 510(k) record lists Devon Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POINT OF USE SHARPS A GATOR?

The FDA product code for POINT OF USE SHARPS A GATOR is FMI.

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Other records listing Devon Industries, Inc. as applicant

K961993BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)K954015ABG POINT LOK NEEDLE PROTECTION DEVICE K946289DEVONS POINT LOK NEEDLE PROTECTION DEVICE K945197THE SHARPS COLLECTION AND DISPOSAL SYSTEM K944114PHLEBOTOMY UNIT SHARPS A GATOR K945485ABG NEEDLE PROTECTION

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Related Devices (Code: FMI)

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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.