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

MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014

K Number: K092232 · Decision Aug 19, 2009
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
10
Review Days
27

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Basic Information

Device Name
MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014
K Number
K092232
Device Class
FDA unclassified
Clearance Type
Special
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Puricore, Inc.
Date Received
July 23, 2009
Decision Date
August 19, 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

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Other Clearances by Puricore, Inc.

K Number Device Name
K141863 PURICORE WOUND HYDROGEL SPRAY DRESSING
K131848 VASHE WOUND SOLUTION (4.0 OZ), (8.5 OZ & (16.0 OZ)
K123072 VASHE WOUND THERAPY SOLUTION
K123071 VASHE SKIN AND WOUND HYDROGEL
K100918 VASHE WOUND THERAPY SYSTEM MODEL: 9000-0014
K093697 VASHE WOUND THERAPY SOLUTION
K093155 VASHE WOUND CLEANSING SYSTEM
K063159 STERILOX LIQUID CHEMICAL STERILANT SYSTEM
K061689 AQUATINE EC ENDODONTIC CLEANSER