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

iRestore

K Number: K151662 · Decision Jan 6, 2016
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
102
Applicant Total
4
Review Days
201

Basic Information

Device Name
iRestore
K Number
K151662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Freedom Laser Therapy, Inc.
Date Received
June 19, 2015
Decision Date
January 6, 2016
Product Code
OAP
Advisory Committee
Physical Medicine
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
OAP Laser, Comb, Hair

Similar 510(k) Clearances

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

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Other Clearances by Freedom Laser Therapy, Inc.

K Number Device Name
K222081 ID-510 iRestore Elite
K213094 ID-500 iRestore Hair Growth System
K183417 iRestore Professional 282