FDA 510(k) FDA unclassified Substantially Equivalent for Some Indications 🇺🇸 United States

DUODERM CGF CONTROL GEL FORMULA DRESSING

K Number: K973632 · Decision Dec 22, 1997
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
81
Review Days
89

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Basic Information

Device Name
DUODERM CGF CONTROL GEL FORMULA DRESSING
K Number
K973632
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent for Some Indications
Applicant
Convatec, A Division of E.R. Squibb & Sons
Date Received
September 24, 1997
Decision Date
December 22, 1997
Product Code
FRO
Advisory Committee
Unknown
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
FRO Dressing, Wound, Drug

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Other Clearances by Convatec, A Division of E.R. Squibb & Sons

K Number Device Name
K013814 ABSORBENT ANTIMICROBIAL WOUND DRESSING
K990964 SIGNADRESS DUODERM DRESSING
K984388 HA ABSORBENT WOUND DRESSING
K980720 NONWOVEN PAD
K980382 NON-WOVEN COMPRESS
K974823 NONWOVEN DRESSING
K974205 KNITTED WOUND DRESSING-STANDARD, WCL AND RIBBON
K974304 GERMICIDAL CLOTH
K972530 CONVATEC ODOR CONTROL WOUND DRESSING
K972062 CONVATEC NON-ADHESIVE DRESSING
Search all 81 clearances from Convatec, A Division of E.R. Squibb & Sons →