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

CHX=CHX PLUS

K Number: K112250 · Decision Oct 28, 2011
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
40
Applicant Total
8
Review Days
85

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Basic Information

Device Name
CHX=CHX PLUS
K Number
K112250
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Inter-Med, Inc.
Date Received
August 4, 2011
Decision Date
October 28, 2011
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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