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

MODEL 5050 SURGILASER FOR NEUROSURGERY USE

K Number: K871933 · Decision Jan 22, 1988
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
8
Review Days
248

Basic Information

Device Name
MODEL 5050 SURGILASER FOR NEUROSURGERY USE
K Number
K871933
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
LASERMATIC, INC.
Date Received
May 19, 1987
Decision Date
January 22, 1988
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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K893529 COMBOLASER MODEL 5050
K871875 MODEL 5050 SURGILASER FOR OB-GYN USE
K871932 MODEL 5050 SURGILASER FOR UROLOGY USE
K871934 MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE
K871876 MODEL 5050 SURGILASER FOR PULMONARY USE