FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

QUADROSTARPROGREEN, QUADROSTARPROYELLOW

K Number: K133297 · Decision Jun 10, 2014
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
20
Review Days
228

Basic Information

Device Name
QUADROSTARPROGREEN, QUADROSTARPROYELLOW
K Number
K133297
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
ASCLEPION LASER TECHNOLOGIES GMBH
Date Received
October 25, 2013
Decision Date
June 10, 2014
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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