PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT)
K-Number: K892291 · 1989-05-11
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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