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

ERCHONIA IOTO_240

K Number: K062792 · Decision Mar 1, 2007
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
72
Applicant Total
9
Review Days
164

Basic Information

Device Name
ERCHONIA IOTO_240
K Number
K062792
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5525
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ERCHONIA MEDICAL, INC.
Date Received
September 18, 2006
Decision Date
March 1, 2007
Product Code
EGJ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EGJ Device, Iontophoresis, Other Uses

Similar 510(k) Clearances

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

View all

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
K120257 MLS, ZERONA-AD
K072206 ERCHONIA EML LASER
K050672 ERCHONIA EVRL LASER
K041139 ERCHONIA EML LASER