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FDA 510(k)

POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES

K-Number: K942149 · 1994-10-13

ApplicantTi-Mate Prophylactic Devices , Ltd.
Decision Date1994-10-13
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES is the device name listed in this FDA 510(k) record. The listed applicant is Ti-Mate Prophylactic Devices , Ltd.. It received FDA 510(k) clearance on 1994-10-13 under 510(k) number K942149. 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 POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES?

POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES is a medical device that received FDA 510(k) clearance on 1994-10-13. The listed applicant is Ti-Mate Prophylactic Devices , Ltd.. The 510(k) number is K942149.

When did POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES receive FDA 510(k) clearance?

POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES received FDA 510(k) clearance on 1994-10-13, under 510(k) number K942149.

Who is the listed applicant for POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES?

The FDA 510(k) record lists Ti-Mate Prophylactic Devices , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES?

The FDA product code for POWDERED DISPOSABLE LATEX EXAM GLOVES/ANNEXURES is LYY.

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Related Devices (Code: LYY)

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Official Source

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