FDA 510(k) FDA class 1 Substantially Equivalent 🇩🇪 Germany

MD 10, SEM, SM 12, CBM

K Number: K000710 · Decision May 11, 2000
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
260
Applicant Total
11
Review Days
70

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Basic Information

Device Name
MD 10, SEM, SM 12, CBM
K Number
K000710
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NOUVAG AG
Date Received
March 2, 2000
Decision Date
May 11, 2000
Product Code
EFB
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
EFB Handpiece, Air-Powered, Dental

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Other Clearances by NOUVAG AG

K Number Device Name
K080365 MORCE POWER PLUS AND VARIOCARVE MORCELLATOR
K081191 TCM ENDO 20
K071588 DISPENSER DP 20
K042822 TCM ENDO V, MODEL 1534
K042943 NOUVAG AG - VACUSON 40 AND VACUSON 60
K042434 MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55
K022505 CONTRA-ANGLE, MODELS 1059, 5050, 5051, 5055, 5056, 5057, 5059, 5060, 5061, 5062, 5063, 5064, 5065, 5066, 5067, 5068,
K013185 TCM ENDO III
K981679 TCM 3000 AND TCM ENDO
K954722 MICRO-DISPENSER 7000 & MICRODISPENSER 8000
Search all 11 clearances from NOUVAG AG →