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

MLS, ZERONA-AD

K Number: K120257 · Decision May 14, 2012
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
32
Applicant Total
10
Review Days
108

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Basic Information

Device Name
MLS, ZERONA-AD
K Number
K120257
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Erchonia Medical, Inc.
Date Received
January 27, 2012
Decision Date
May 14, 2012
Product Code
OLI
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
OLI Fat Reducing Low Level Laser

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Other Clearances by Erchonia Medical, Inc.

K Number Device Name
K153164 LunulaLaser
K132940 ERCHONIA ALLAY
K130996 ERCHONIA EMERGE
K130922 ERCHONIA VERJU LASER SYSTEM WITH MASSAGER
K130741 ERCHONIA PL5000
K072206 ERCHONIA EML LASER
K062792 ERCHONIA IOTO_240
K050672 ERCHONIA EVRL LASER
K041139 ERCHONIA EML LASER