FDA 510(k)

TA TA LATEX EXAM GLOVE

K-Number: K892365 · 1989-04-26

Decision Date1989-04-26

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

TA TA LATEX EXAM GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Ta TA Industrial Co., Ltd.. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K892365. 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 TA TA LATEX EXAM GLOVE?

TA TA LATEX EXAM GLOVE is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Ta TA Industrial Co., Ltd.. The 510(k) number is K892365.

When did TA TA LATEX EXAM GLOVE receive FDA 510(k) clearance?

TA TA LATEX EXAM GLOVE received FDA 510(k) clearance on 1989-04-26, under 510(k) number K892365.

Who is the listed applicant for TA TA LATEX EXAM GLOVE?

The FDA 510(k) record lists Ta TA Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TA TA LATEX EXAM GLOVE?

The FDA product code for TA TA LATEX EXAM GLOVE is 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.