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

LaserCap Family of Lasers 300, 224, 120 & 80

K Number: K203826 · Decision Mar 29, 2021
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
102
Applicant Total
1
Review Days
90

Basic Information

Device Name
LaserCap Family of Lasers 300, 224, 120 & 80
K Number
K203826
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Transdermal Cap, Inc.
Date Received
December 29, 2020
Decision Date
March 29, 2021
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

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