PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)— 510(k) K893072

Name: FDA 510(k) clearance K893072
Creator: U.S. Food and Drug Administration
Published: 1990-05-18

Substantially Equivalent

Innovative Medical Suppliers

FDA 510(k) clearance K893072 for PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.), Substantially Equivalent on 1990-05-18. Applicant: Innovative Medical Suppliers. Device class: 1.

Clearance details

Applicant: Innovative Medical Suppliers
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-04-13
Decision date: 1990-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cardiff, CA, US

Download summary PDF View on FDA.gov ↗

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