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

SilverSeal

K Number: K171041 · Decision Aug 22, 2017
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
2
Review Days
137

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Basic Information

Device Name
SilverSeal
K Number
K171041
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alliqua Biomedical, Inc.
Date Received
April 7, 2017
Decision Date
August 22, 2017
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 Alliqua Biomedical, Inc.

K Number Device Name
K162721 Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator