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

AQUATINE EC ENDODONTIC CLEANSER

K Number: K061689 · Decision Aug 24, 2006
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
40
Applicant Total
10
Review Days
70

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Basic Information

Device Name
AQUATINE EC ENDODONTIC CLEANSER
K Number
K061689
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Puricore, Inc.
Date Received
June 15, 2006
Decision Date
August 24, 2006
Product Code
KJJ
Advisory Committee
Unknown
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KJJ Cleanser, Root Canal

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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
K092232 MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014
K063159 STERILOX LIQUID CHEMICAL STERILANT SYSTEM