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FDA 510(k)

SURGEON'S GLOVES

K-Number: K893522 · 1990-01-22

ApplicantThai Fuji Latex Co., Ltd.
Decision Date1990-01-22
Product CodeFGO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGEON'S GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Thai Fuji Latex Co., Ltd.. It received FDA 510(k) clearance on 1990-01-22 under 510(k) number K893522. The device is classified under product code FGO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGEON'S GLOVES?

SURGEON'S GLOVES is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Thai Fuji Latex Co., Ltd.. The 510(k) number is K893522.

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

SURGEON'S GLOVES received FDA 510(k) clearance on 1990-01-22, under 510(k) number K893522.

Who is the listed applicant for SURGEON'S GLOVES?

The FDA 510(k) record lists Thai Fuji Latex Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for SURGEON'S GLOVES is FGO.

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Related Devices (Code: FGO)

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

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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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