FDA 510(k)

BIOSHIELD BLUE POWDER FREE GLOVE

K-Number: K940254 · 1994-03-23

Decision Date1994-03-23

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BIOSHIELD BLUE POWDER FREE GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Chester Labs, Inc.. It received FDA 510(k) clearance on 1994-03-23 under 510(k) number K940254. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOSHIELD BLUE POWDER FREE GLOVE?

BIOSHIELD BLUE POWDER FREE GLOVE is a medical device that received FDA 510(k) clearance on 1994-03-23. The listed applicant is Chester Labs, Inc.. The 510(k) number is K940254.

When did BIOSHIELD BLUE POWDER FREE GLOVE receive FDA 510(k) clearance?

BIOSHIELD BLUE POWDER FREE GLOVE received FDA 510(k) clearance on 1994-03-23, under 510(k) number K940254.

Who is the listed applicant for BIOSHIELD BLUE POWDER FREE GLOVE?

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

What is the FDA product code for BIOSHIELD BLUE POWDER FREE GLOVE?

The FDA product code for BIOSHIELD BLUE POWDER FREE GLOVE is LYY.

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Related Devices (Code: LYY)

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Official Source

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