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

AQUACEL HYDROFIBER WOUND DRESSING

K Number: K982116 · Decision Sep 8, 1998
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
10
Review Days
84

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Basic Information

Device Name
AQUACEL HYDROFIBER WOUND DRESSING
K Number
K982116
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Convatec, A Bristol-Myers Squibb Co.
Date Received
June 16, 1998
Decision Date
September 8, 1998
Product Code
KMF
Advisory Committee
General Hospital
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
KMF Bandage, Liquid

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KMF), ordered by most recent decision date.

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Other Clearances by Convatec, A Bristol-Myers Squibb Co.

K Number Device Name
K032734 CONVATEC FECAL MANAGEMENT SYSTEM
K990368 DUODERM HYDROACTIVE GEL WOUND DRESSING
K973806 DUODERM HYDROACTIVE GEL
K973807 DUODERM HYDROACTIVE PASTE
K973716 DUODERM EXTRA THIN CGF DRESSING
K973717 COMBIDERM ACD
K954918 COMBIDERM ACD
K942941 CONQUEST MALE CONTINENCE SYSTEM
K940895 EPIVIEW