Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green

K-Number: K202085 · 2021-06-21

Decision Date2021-06-21
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green is a medical device manufactured by Shen Wei USA, Inc.. It received FDA 510(k) clearance on 2021-06-21 under approval number K202085. 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 Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green?

Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green is a medical device that received FDA 510(k) clearance on 2021-06-21. It is manufactured by Shen Wei USA, Inc.. The 510(k) number is K202085.

When was Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green approved by the FDA?

Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green received FDA 510(k) clearance on 2021-06-21, under approval number K202085.

What company makes Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green?

Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green is manufactured by Shen Wei USA, Inc..

What is the FDA product code for Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green?

The FDA product code for Biodegradable Powder Free Neoprene Examination Glove, Low Dermatitis Potential Claim, Green is LZA.

Related Clinical Trials

Related PubMed Literature

Other Devices by Shen Wei USA, Inc.

View all 18 devices →

Related Devices (Code: LZA)

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.