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

WATERLASE C100, MODEL 7100104

K Number: K091922 · Decision Jul 14, 2009
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
31
Review Days
14

Basic Information

Device Name
WATERLASE C100, MODEL 7100104
K Number
K091922
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIOLASE TECHNOLOGY, INC.
Date Received
June 30, 2009
Decision Date
July 14, 2009
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEX Powered Laser Surgical Instrument

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