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

MASTERSCALE II

K Number: K791704 · Decision Oct 26, 1979
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
191
Applicant Total
12
Review Days
59

Basic Information

Device Name
MASTERSCALE II
K Number
K791704
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4850
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
LITTON DENTAL PRODUCTS
Date Received
August 28, 1979
Decision Date
October 26, 1979
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
K791024 ULTRASONIC DENTAL PROPHYLAXIS UNIT
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K772244 ILLUMINATED DENTAL HANDPIECE
K771556 EXR
K771557 ULTRASON 990
K771252 CB600, TURBINE CONTROL BOL
K771251 HU:500, HYGIENASSIST
K761246 SONUS III
K761247 LT:200, LOVING TOUCH
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