FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ABSORBENT GAUZE ROLL

K Number: K890672 · Decision Apr 7, 1989
Classifications
1
FEI Numbers
570
Registration Numbers
570
Same Product Code
87
Applicant Total
34
Review Days
57

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Basic Information

Device Name
ABSORBENT GAUZE ROLL
K Number
K890672
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4014
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Smith & Nephew United, Inc.
Date Received
February 9, 1989
Decision Date
April 7, 1989
Product Code
NAB
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NAB Gauze / Sponge,Nonresorbable For External Use

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K943619 CAVI-CARE CONFORMING FOAM DRESSING
K942748 INTRASITE
K935705 ALLEVYN ISLAND WOUND DRESSING
K935803 CICA-CARE SILICONE GEL SHEET
K932263 SOLOSITE DERMAL WOUND GEL
K926508 INTRASITE GEL
K922897 STRAPPAL
Search all 34 clearances from Smith & Nephew United, Inc. →