FDA 510(k) FDA unclassified Substantially Equivalent 🇨🇦 Canada

EXSALT SD7 WOUND DRESSING

K Number: K083870 · Decision Jul 30, 2009
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
7
Review Days
213

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EXSALT SD7 WOUND DRESSING
K Number
K083870
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Exciton Technologies, Inc.
Date Received
December 29, 2008
Decision Date
July 30, 2009
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

Similar 510(k) Clearances

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

View all

Other Clearances by Exciton Technologies, Inc.

K Number Device Name
K182680 KerraContact Ag Perf Advanced Perforated Silver Wound Dressing
K162508 KerraCel Ag Gelling Fiber Silver Dressing
K133775 EXSALT SD7 WOUND DRESSING WITH ADHESIVE BACKING
K113564 EXSALT T7 WOUND DRESSING
K103067 EXSALT SD7 WOUND DRESSING
K100580 EXSALT WOUND DRESSING