FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇭 Switzerland

CONTRA-ANGLE, MODELS 1059, 5050, 5051, 5055, 5056, 5057, 5059, 5060, 5061, 5062, 5063, 5064, 5065, 5066, 5067, 5068,

K Number: K022505 · Decision Oct 1, 2003
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
72
Applicant Total
11
Review Days
429

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Basic Information

Device Name
CONTRA-ANGLE, MODELS 1059, 5050, 5051, 5055, 5056, 5057, 5059, 5060, 5061, 5062, 5063, 5064, 5065, 5066, 5067, 5068,
K Number
K022505
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
July 29, 2002
Decision Date
October 1, 2003
Product Code
EGS
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
EGS Handpiece, Contra- And Right-Angle Attachment, 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
K013185 TCM ENDO III
K000710 MD 10, SEM, SM 12, CBM
K981679 TCM 3000 AND TCM ENDO
K954722 MICRO-DISPENSER 7000 & MICRODISPENSER 8000
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