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FDA 510(k)

PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT)

K-Number: K892291 · 1989-05-11

Decision Date1989-05-11
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT) is the device name listed in this FDA 510(k) record. The listed applicant is American Health Products, Inc.. It received FDA 510(k) clearance on 1989-05-11 under 510(k) number K892291. 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 PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT)?

PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT) is a medical device that received FDA 510(k) clearance on 1989-05-11. The listed applicant is American Health Products, Inc.. The 510(k) number is K892291.

When did PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT) receive FDA 510(k) clearance?

PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT) received FDA 510(k) clearance on 1989-05-11, under 510(k) number K892291.

Who is the listed applicant for PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT)?

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

What is the FDA product code for PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT)?

The FDA product code for PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT) 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 American Health Products, 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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