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

R7

K Number: K130834 · Decision Oct 8, 2013
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
194
Applicant Total
21
Review Days
196

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Basic Information

Device Name
R7
K Number
K130834
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4850
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cefla S.C.
Date Received
March 26, 2013
Decision Date
October 8, 2013
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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K231990 Apex Locator
K223794 hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS
K213022 CEFLA Dental Micromotors: i-MMr, i-MMr L, i-MMs, i-XR3, i-XR3 L, i-XS4, handy POWER, handy POWER LED, implantor LED
K220664 NewTom 7G
K214084 hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS
K200688 hyperion X5, NewTom GO, X-RADiUS COMPACT
K190496 hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS
Search all 21 clearances from Cefla S.C. →