FDA 510(k)

NITRILE EXAM GLOVE, POWDER-FREE, BLUE

K-Number: K980802 · 1998-03-25

Decision Date1998-03-25

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NITRILE EXAM GLOVE, POWDER-FREE, BLUE is the device name listed in this FDA 510(k) record. The listed applicant is Tucker & Associates. It received FDA 510(k) clearance on 1998-03-25 under 510(k) number K980802. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NITRILE EXAM GLOVE, POWDER-FREE, BLUE?

NITRILE EXAM GLOVE, POWDER-FREE, BLUE is a medical device that received FDA 510(k) clearance on 1998-03-25. The listed applicant is Tucker & Associates. The 510(k) number is K980802.

When did NITRILE EXAM GLOVE, POWDER-FREE, BLUE receive FDA 510(k) clearance?

NITRILE EXAM GLOVE, POWDER-FREE, BLUE received FDA 510(k) clearance on 1998-03-25, under 510(k) number K980802.

Who is the listed applicant for NITRILE EXAM GLOVE, POWDER-FREE, BLUE?

The FDA 510(k) record lists Tucker & Associates as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NITRILE EXAM GLOVE, POWDER-FREE, BLUE?

The FDA product code for NITRILE EXAM GLOVE, POWDER-FREE, BLUE is LZA.

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Other records listing Tucker & Associates as applicant

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Related Devices (Code: LZA)

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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.