FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

Surgical laser fibers

K Number: K200234 · Decision Feb 25, 2020
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
9
Review Days
26

Basic Information

Device Name
Surgical laser fibers
K Number
K200234
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
Quanta System Spa
Date Received
January 30, 2020
Decision Date
February 25, 2020
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEX), ordered by most recent decision date.

View all

Other Clearances by Quanta System Spa

K Number Device Name
K232236 Echo
K220426 Fiber Dust PRO
K210142 Fiber Dust
K202503 Chrome
K201455 Litho 150, Cyber Ho 150
K181632 Venacure 1470 Pro
K180426 Empower H35
K163222 Discovery Pico Family