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FDA 510(k)

STERILE DISPOSABLE SURGICAL GLOVES

K-Number: K812421 · 1982-02-10

Decision Date1982-02-10
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE DISPOSABLE SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Intermarket Latex, Inc.. It received FDA 510(k) clearance on 1982-02-10 under 510(k) number K812421. 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 DISPOSABLE SURGICAL GLOVES?

STERILE DISPOSABLE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1982-02-10. The listed applicant is Intermarket Latex, Inc.. The 510(k) number is K812421.

When did STERILE DISPOSABLE SURGICAL GLOVES receive FDA 510(k) clearance?

STERILE DISPOSABLE SURGICAL GLOVES received FDA 510(k) clearance on 1982-02-10, under 510(k) number K812421.

Who is the listed applicant for STERILE DISPOSABLE SURGICAL GLOVES?

The FDA 510(k) record lists Intermarket Latex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE DISPOSABLE SURGICAL GLOVES?

The FDA product code for STERILE DISPOSABLE 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.

Other records listing Intermarket Latex, Inc. 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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