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

P-NAIN SYSTEM

K Number: K072833 · Decision Jan 24, 2008
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
6
Review Days
113

Basic Information

Device Name
P-NAIN SYSTEM
K Number
K072833
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
JEISYS MEDICAL, INC.
Date Received
October 3, 2007
Decision Date
January 24, 2008
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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