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FDA 510(k)

PROTEQ SURGEON'S GLOVES

K-Number: K880632 · 1988-03-31

Decision Date1988-03-31
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROTEQ SURGEON'S GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Strategic Materials Group. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K880632. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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