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FDA 510(k)

LATEX EXAMINATION GLOVE POWDER FREE

K-Number: K152593 · 2016-02-25

Decision Date2016-02-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVE POWDER FREE is a medical device manufactured by Careplus (M) Sdn Bhd. It received FDA 510(k) clearance on 2016-02-25 under approval number K152593. 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 LATEX EXAMINATION GLOVE POWDER FREE?

LATEX EXAMINATION GLOVE POWDER FREE is a medical device that received FDA 510(k) clearance on 2016-02-25. It is manufactured by Careplus (M) Sdn Bhd. The 510(k) number is K152593.

When was LATEX EXAMINATION GLOVE POWDER FREE approved by the FDA?

LATEX EXAMINATION GLOVE POWDER FREE received FDA 510(k) clearance on 2016-02-25, under approval number K152593.

What company makes LATEX EXAMINATION GLOVE POWDER FREE?

LATEX EXAMINATION GLOVE POWDER FREE is manufactured by Careplus (M) Sdn Bhd.

What is the FDA product code for LATEX EXAMINATION GLOVE POWDER FREE?

The FDA product code for LATEX EXAMINATION GLOVE POWDER FREE 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.