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

MOSAIC ECO2 LASER SYSTEM

K Number: K080496 · Decision Jul 7, 2008
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
19
Review Days
136

Basic Information

Device Name
MOSAIC ECO2 LASER SYSTEM
K Number
K080496
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
LUTRONIC CORPORATION
Date Received
February 22, 2008
Decision Date
July 7, 2008
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 LUTRONIC CORPORATION

K Number Device Name
K163196 ACTION II Laser System
K141555 ADVANTAGE
K130199 CLARITY LPC LASER SYSTEM
K121481 INFINI RADIOFREQUENCY SYSTEM
K113843 FREEDOM ND: YAG LASER SYSTEM
K113668 HEALITE II SYSTEM
K113502 ADVANTAGE LASER SYSTEM
K113588 SPECTRA LASER SYSTEM
K103455 SPECTRA LASER SYSTEM
K100610 LUTRONIC CORPORATION ECO2 PLUS, DENTA III AND III+ AND SP III LASER SYSTEMS
Search all 19 clearances from LUTRONIC CORPORATION →