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FDA 510(k)

STERILE & NON-STERILE SURGEONS GLOVES

K-Number: K882200 · 1989-02-03

Decision Date1989-02-03
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE & NON-STERILE SURGEONS GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Taroko Ent., Ltd.. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K882200. 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 STERILE & NON-STERILE SURGEONS GLOVES?

STERILE & NON-STERILE SURGEONS GLOVES is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Taroko Ent., Ltd.. The 510(k) number is K882200.

When did STERILE & NON-STERILE SURGEONS GLOVES receive FDA 510(k) clearance?

STERILE & NON-STERILE SURGEONS GLOVES received FDA 510(k) clearance on 1989-02-03, under 510(k) number K882200.

Who is the listed applicant for STERILE & NON-STERILE SURGEONS GLOVES?

The FDA 510(k) record lists Taroko Ent., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE & NON-STERILE SURGEONS GLOVES?

The FDA product code for STERILE & NON-STERILE SURGEONS 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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