POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K-Number: K992272 · 1999-10-01
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1999-10-01. The listed applicant is Shanghai Cosmos Corp.. The 510(k) number is K992272.
When did POWDER-FREE VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1999-10-01, under 510(k) number K992272.
Who is the listed applicant for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Shanghai Cosmos Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?
The FDA product code for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES is LYZ.
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.
Other records listing Shanghai Cosmos Corp. as applicant
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: LYZ)
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
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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