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

MultiPulse HoPLUS

K Number: K161257 · Decision Mar 31, 2017
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
20
Review Days
331

Basic Information

Device Name
MultiPulse HoPLUS
K Number
K161257
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
ASCLEPION LASER TECHNOLOGIES GMBH
Date Received
May 4, 2016
Decision Date
March 31, 2017
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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K113489 ORION
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