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

VISULAS 532S

K Number: K013402 · Decision Nov 14, 2001
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
44
Review Days
30

Basic Information

Device Name
VISULAS 532S
K Number
K013402
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
CARL ZEISS, INC.
Date Received
October 15, 2001
Decision Date
November 14, 2001
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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