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FDA 510(k)

SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS

K-Number: K900985 · 1990-03-20

Decision Date1990-03-20
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS is the device name listed in this FDA 510(k) record. The listed applicant is Productes Del Latex, S.A.. It received FDA 510(k) clearance on 1990-03-20 under 510(k) number K900985. 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 SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS?

SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS is a medical device that received FDA 510(k) clearance on 1990-03-20. The listed applicant is Productes Del Latex, S.A.. The 510(k) number is K900985.

When did SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS receive FDA 510(k) clearance?

SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS received FDA 510(k) clearance on 1990-03-20, under 510(k) number K900985.

Who is the listed applicant for SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS?

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

What is the FDA product code for SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS?

The FDA product code for SURGEONS' GLOVES W/HYPOALLERGENICITY CLAIMS 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 Productes Del Latex, S.A. 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.

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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