FDA 510(k) K803293, GUARDIAN PEEL POUCHES, KIMBERLY-CLARK CORP.
FDA 510(k) K803293, GUARDIAN PEEL POUCHES, KIMBERLY-CLARK CORP.
Device Name: GUARDIAN PEEL POUCHES
Manufacturer: KIMBERLY-CLARK CORP.
Device Classification Name: Wrap, Sterilization
Regulation Number: 880.6850
Classification Product Code: FRG
Date Received: 12/30/1980
Decision Date: 01/28/1981
Regulation Medical Specialty: General Hospital
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