FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

RESURFX 1565NM LASER MODULE

K Number: K130028 · Decision Sep 3, 2013
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
34
Applicant Total
28
Review Days
243

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Basic Information

Device Name
RESURFX 1565NM LASER MODULE
K Number
K130028
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
Lumenis, Ltd.
Date Received
January 3, 2013
Decision Date
September 3, 2013
Product Code
ONG
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
ONG Powered Laser Surgical Instrument With MicrobeamFractional Output

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