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

LunulaLaser

K Number: K153164 · Decision Jun 3, 2016
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
18
Applicant Total
10
Review Days
214

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Basic Information

Device Name
LunulaLaser
K Number
K153164
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Erchonia Medical, Inc.
Date Received
November 2, 2015
Decision Date
June 3, 2016
Product Code
PDZ
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
PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis

Similar 510(k) Clearances

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

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Other Clearances by Erchonia Medical, Inc.

K Number Device Name
K132940 ERCHONIA ALLAY
K130996 ERCHONIA EMERGE
K130922 ERCHONIA VERJU LASER SYSTEM WITH MASSAGER
K130741 ERCHONIA PL5000
K120257 MLS, ZERONA-AD
K072206 ERCHONIA EML LASER
K062792 ERCHONIA IOTO_240
K050672 ERCHONIA EVRL LASER
K041139 ERCHONIA EML LASER