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FDA 510(k)

Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)

K-Number: K221350 · 2022-08-05

Decision Date2022-08-05
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) is the device name listed in this FDA 510(k) record. The listed applicant is Rubberex Alliance Products Sdn Bhd. It received FDA 510(k) clearance on 2022-08-05 under 510(k) number K221350. 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 Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)?

Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) is a medical device that received FDA 510(k) clearance on 2022-08-05. The listed applicant is Rubberex Alliance Products Sdn Bhd. The 510(k) number is K221350.

When did Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) receive FDA 510(k) clearance?

Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) received FDA 510(k) clearance on 2022-08-05, under 510(k) number K221350.

Who is the listed applicant for Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)?

The FDA 510(k) record lists Rubberex Alliance Products Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)?

The FDA product code for Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) is LZA.

Related Clinical Trials

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.

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