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

PREMIER ULTRASONIC SCALER AND INSERTS

K Number: K010195 · Decision Apr 17, 2001
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
194
Applicant Total
41
Review Days
85

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Basic Information

Device Name
PREMIER ULTRASONIC SCALER AND INSERTS
K Number
K010195
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4850
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Premier Dental Products Co.
Date Received
January 22, 2001
Decision Date
April 17, 2001
Product Code
ELC
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
ELC Scaler, Ultrasonic

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K062683 ENAMEL PRO VARNISH
K062166 ENAMEL PRO
K061997 PREMIER SELF-ETCHING ENAMEL SEALANT
K061998 PREMIER SELF-ETCHING BOND ENHANCER
K051866 PREMIER TEMPORARY CEMENT
K042215 RADIOPAQUE, GLASS IONOMER ENDODONTIC CEMENT
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