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FDA 510(k)

Nitrile Patient Examination Gloves, Powder Free

K-Number: K220697 · 2022-09-15

ApplicantLalan Rubbers (Pvt), Ltd.
Decision Date2022-09-15
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Nitrile Patient Examination Gloves, Powder Free is a medical device manufactured by Lalan Rubbers (Pvt), Ltd.. It received FDA 510(k) clearance on 2022-09-15 under approval number K220697. 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 Patient Examination Gloves, Powder Free?

Nitrile Patient Examination Gloves, Powder Free is a medical device that received FDA 510(k) clearance on 2022-09-15. It is manufactured by Lalan Rubbers (Pvt), Ltd.. The 510(k) number is K220697.

When was Nitrile Patient Examination Gloves, Powder Free approved by the FDA?

Nitrile Patient Examination Gloves, Powder Free received FDA 510(k) clearance on 2022-09-15, under approval number K220697.

What company makes Nitrile Patient Examination Gloves, Powder Free?

Nitrile Patient Examination Gloves, Powder Free is manufactured by Lalan Rubbers (Pvt), Ltd..

What is the FDA product code for Nitrile Patient Examination Gloves, Powder Free?

The FDA product code for Nitrile Patient Examination Gloves, Powder Free 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.

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