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FDA 510(k)

ANGEL LATEX SURGICAL GLOVES

K-Number: K864521 · 1986-12-18

Decision Date1986-12-18
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANGEL LATEX SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Kim Intl. Trading Co.. It received FDA 510(k) clearance on 1986-12-18 under 510(k) number K864521. 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 ANGEL LATEX SURGICAL GLOVES?

ANGEL LATEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1986-12-18. The listed applicant is Kim Intl. Trading Co.. The 510(k) number is K864521.

When did ANGEL LATEX SURGICAL GLOVES receive FDA 510(k) clearance?

ANGEL LATEX SURGICAL GLOVES received FDA 510(k) clearance on 1986-12-18, under 510(k) number K864521.

Who is the listed applicant for ANGEL LATEX SURGICAL GLOVES?

The FDA 510(k) record lists Kim Intl. Trading Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANGEL LATEX SURGICAL GLOVES?

The FDA product code for ANGEL LATEX SURGICAL 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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