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FDA 510(k)

Nitrile Patient Examination Gloves, Powder Free

K-Number: K220697 · 2022-09-15

Decision Date2022-09-15
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Nitrile Patient Examination Gloves, Powder Free is the device name listed in this FDA 510(k) record. The listed applicant is Lalan Rubbers (Pvt), Ltd.. It received FDA 510(k) clearance on 2022-09-15 under 510(k) 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. The listed applicant is Lalan Rubbers (Pvt), Ltd.. The 510(k) number is K220697.

When did Nitrile Patient Examination Gloves, Powder Free receive FDA 510(k) clearance?

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

Who is the listed applicant for Nitrile Patient Examination Gloves, Powder Free?

The FDA 510(k) record lists Lalan Rubbers (Pvt), Ltd. as the applicant. This does not by itself establish the device manufacturer.

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.

Related Devices (Code: LZA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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