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FDA 510(k)

DURAPRENE STERILE SYNTHETIC SURGEON'S GLOVES

K-Number: K941770 · 1994-07-05

Decision Date1994-07-05
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DURAPRENE STERILE SYNTHETIC SURGEON'S GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1994-07-05 under 510(k) number K941770. 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 DURAPRENE STERILE SYNTHETIC SURGEON'S GLOVES?

DURAPRENE STERILE SYNTHETIC SURGEON'S GLOVES is a medical device that received FDA 510(k) clearance on 1994-07-05. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K941770.

When did DURAPRENE STERILE SYNTHETIC SURGEON'S GLOVES receive FDA 510(k) clearance?

DURAPRENE STERILE SYNTHETIC SURGEON'S GLOVES received FDA 510(k) clearance on 1994-07-05, under 510(k) number K941770.

Who is the listed applicant for DURAPRENE STERILE SYNTHETIC SURGEON'S GLOVES?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DURAPRENE STERILE SYNTHETIC SURGEON'S GLOVES?

The FDA product code for DURAPRENE STERILE SYNTHETIC 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.

Other records listing Baxter Healthcare 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.

View all 504 devices →

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

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