FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ALL-ETCH, ALL- ETCH WITH BAC; UNI- ETCH, UNI- ETCH WITH BAC; ETCH- 37, ETCH- 37 WITH BAC; DARK- ETCH, DARK ETCH (BLUE- E

K Number: K101485 · Decision Aug 26, 2010
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
88
Review Days
90

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Basic Information

Device Name
ALL-ETCH, ALL- ETCH WITH BAC; UNI- ETCH, UNI- ETCH WITH BAC; ETCH- 37, ETCH- 37 WITH BAC; DARK- ETCH, DARK ETCH (BLUE- E
K Number
K101485
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bisco, Inc.
Date Received
May 28, 2010
Decision Date
August 26, 2010
Product Code
KLE
Advisory Committee
Dental
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
KLE Agent, Tooth Bonding, Resin

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K171147 REVEAL Bulk
K162598 HAPI Seal
K163171 CeraClean
K161051 All-Bond Universal w/BAC (not finalized)
K161256 TheraCem
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