PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT)— 510(k) K892291

Substantially Equivalent

American Health Products, Inc.

FDA 510(k) clearance K892291 for PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT), Substantially Equivalent on 1989-05-11. Applicant: American Health Products, Inc.. Device class: 1.

Clearance details

Applicant
American Health Products, Inc.
Product code
Code LYY
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
North Brook, IL, US
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