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

INTRALASE FS LASER

K Number: K031960 · Decision Sep 29, 2003
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
8
Review Days
96

Basic Information

Device Name
INTRALASE FS LASER
K Number
K031960
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
INTRALASE CORP.
Date Received
June 25, 2003
Decision Date
September 29, 2003
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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Other Clearances by INTRALASE CORP.

K Number Device Name
K073404 IFS LASER SYSTEM
K063682 INTRALASE FUSION LASER
K041893 INTRALASE FS LASER
K013941 PULSION FS LASER KERATOME
K002890 INTRALASE 600C LASER KERATOME
K001211 MODIFICATION TO INTRALASE 600C LASER KERATOME
K993153 INTRALASE 600C LASER KERATOME