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

SONUS III

K Number: K761246 · Decision Dec 16, 1976
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
194
Applicant Total
12
Review Days
3

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Basic Information

Device Name
SONUS III
K Number
K761246
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4850
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Litton Dental Products
Date Received
December 13, 1976
Decision Date
December 16, 1976
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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Other Clearances by Litton Dental Products

K Number Device Name
K791704 MASTERSCALE II
K791024 ULTRASONIC DENTAL PROPHYLAXIS UNIT
K781114 ULTRAMATE 990
K781044 ULTRASONIC DENTAL PROPHYLAXIS UNIT,SSM
K772244 ILLUMINATED DENTAL HANDPIECE
K771556 EXR
K771557 ULTRASON 990
K771251 HU:500, HYGIENASSIST
K771252 CB600, TURBINE CONTROL BOL
K761247 LT:200, LOVING TOUCH
Search all 12 clearances from Litton Dental Products →