FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

IS 40 MICROMOTOR

K Number: K042787 · Decision Dec 17, 2004
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
260
Applicant Total
24
Review Days
72

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Basic Information

Device Name
IS 40 MICROMOTOR
K Number
K042787
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Satelec
Date Received
October 6, 2004
Decision Date
December 17, 2004
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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K071965 I-SURGE
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