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

AQUACEL AG EXTRA HYDROFIBER DRESSING WITH SILVER AND STRENGTHENING FIBER

K Number: K121275 · Decision Jul 25, 2012
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
7
Review Days
89

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Basic Information

Device Name
AQUACEL AG EXTRA HYDROFIBER DRESSING WITH SILVER AND STRENGTHENING FIBER
K Number
K121275
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Convatec, Inc.
Date Received
April 27, 2012
Decision Date
July 25, 2012
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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K Number Device Name
K230400 Cure Catheter Closed System; Cure Dextra Closed System
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K123481 AQUACEL AG FOAM HYDROFIBER FOAM DRESSING WITH SILVER, ADHESIVE AND NON ADHESIVE
K112342 FLEXI-SEAL SIGNAL FECAL MANAGEMENT SYSTEM
K111365 VITALA CONTINENCE CONTROL DEVICE
K102536 VITALA CONTINENCE CONTROL DEVICE