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FDA 510(k)

POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED)

K-Number: K172015 · 2017-09-26

Decision Date2017-09-26
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED) is a medical device manufactured by Careglove Global Sdn. Bhd.. It received FDA 510(k) clearance on 2017-09-26 under approval number K172015. 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 POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED)?

POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED) is a medical device that received FDA 510(k) clearance on 2017-09-26. It is manufactured by Careglove Global Sdn. Bhd.. The 510(k) number is K172015.

When was POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED) approved by the FDA?

POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED) received FDA 510(k) clearance on 2017-09-26, under approval number K172015.

What company makes POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED)?

POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED) is manufactured by Careglove Global Sdn. Bhd..

What is the FDA product code for POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED)?

The FDA product code for POWDER FREE NITRILE EXAMINATION GLOVES, BLUE (COLORED) is LZA.

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Official Source

View on FDA Database →

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