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FDA 510(k)

LATEX NON-STERILE EXAM GLOVES

K-Number: K890496 · 1989-04-28

Decision Date1989-04-28
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX NON-STERILE EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Cal-American Exports, Inc.. It received FDA 510(k) clearance on 1989-04-28 under 510(k) number K890496. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATEX NON-STERILE EXAM GLOVES?

LATEX NON-STERILE EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-28. The listed applicant is Cal-American Exports, Inc.. The 510(k) number is K890496.

When did LATEX NON-STERILE EXAM GLOVES receive FDA 510(k) clearance?

LATEX NON-STERILE EXAM GLOVES received FDA 510(k) clearance on 1989-04-28, under 510(k) number K890496.

Who is the listed applicant for LATEX NON-STERILE EXAM GLOVES?

The FDA 510(k) record lists Cal-American Exports, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX NON-STERILE EXAM GLOVES?

The FDA product code for LATEX NON-STERILE EXAM GLOVES is LYY.

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 Cal-American Exports, 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: LYY)

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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