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

H-30 HOLMIUM LASER SYSTEM

K Number: K130444 · Decision May 22, 2013
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
190
Review Days
90

Basic Information

Device Name
H-30 HOLMIUM LASER SYSTEM
K Number
K130444
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
COOK, INC.
Date Received
February 21, 2013
Decision Date
May 22, 2013
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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