PROTEQ SURGEON'S GLOVES
K-Number: K880632 · 1988-03-31
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Device Summary
Frequently Asked Questions
What is the PROTEQ SURGEON'S GLOVES?
PROTEQ SURGEON'S GLOVES is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Strategic Materials Group. The 510(k) number is K880632.
When did PROTEQ SURGEON'S GLOVES receive FDA 510(k) clearance?
PROTEQ SURGEON'S GLOVES received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880632.
Who is the listed applicant for PROTEQ SURGEON'S GLOVES?
The FDA 510(k) record lists Strategic Materials Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTEQ SURGEON'S GLOVES?
The FDA product code for PROTEQ SURGEON'S GLOVES is KGO.
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: KGO)
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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