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

PicoLazer Laser System

K Number: K192583 · Decision Jan 17, 2020
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
6
Review Days
120

Basic Information

Device Name
PicoLazer Laser System
K Number
K192583
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
Rohrer Aesthetics, LLC
Date Received
September 19, 2019
Decision Date
January 17, 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 Rohrer Aesthetics, LLC

K Number Device Name
K233099 Gladiator
K212331 BodySculp
K210535 UltraLight LED System
K191162 EpiLaze Multi-wavelength Laser
K180654 PINXEL-RF system