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FDA 510(k)

GLOVES, STERILE LATEX SURGEON'S

K-Number: K760243 · 1976-08-03

ApplicantTravenol Laboratories, S.A.
Decision Date1976-08-03
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GLOVES, STERILE LATEX SURGEON'S is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1976-08-03 under 510(k) number K760243. 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 GLOVES, STERILE LATEX SURGEON'S?

GLOVES, STERILE LATEX SURGEON'S is a medical device that received FDA 510(k) clearance on 1976-08-03. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K760243.

When did GLOVES, STERILE LATEX SURGEON'S receive FDA 510(k) clearance?

GLOVES, STERILE LATEX SURGEON'S received FDA 510(k) clearance on 1976-08-03, under 510(k) number K760243.

Who is the listed applicant for GLOVES, STERILE LATEX SURGEON'S?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLOVES, STERILE LATEX SURGEON'S?

The FDA product code for GLOVES, STERILE LATEX SURGEON'S is KGO.

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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.

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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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