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

MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL

K Number: K060270 · Decision Apr 10, 2006
Classifications
1
FEI Numbers
76
Registration Numbers
76
Same Product Code
46
Applicant Total
93
Review Days
68

Basic Information

Device Name
MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL
K Number
K060270
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.4120
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LINVATEC CORP.
Date Received
February 1, 2006
Decision Date
April 10, 2006
Product Code
DZI
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
DZI Drill, Bone, Powered

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