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

ECLIPSE 3200 FOR USE IN UROLOGY APPLICATIONS

K Number: K931305 · Decision Jan 7, 1994
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
20
Review Days
298

Basic Information

Device Name
ECLIPSE 3200 FOR USE IN UROLOGY APPLICATIONS
K Number
K931305
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
CARDIOGENES
Date Received
March 15, 1993
Decision Date
January 7, 1994
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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