LaserCap300, LaserCap224, LaserCap120, LaserCap80

FDA 510(k) K161875 · Transdermal Cap, Inc.

Substantially Equivalent

510(k) numberK161875

Submission

Device name
LaserCap300, LaserCap224, LaserCap120, LaserCap80
Applicant
Transdermal Cap, Inc.
Gates Mills, OH, US
Received
July 8, 2016
Decision date
September 30, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OAP – Laser, Comb, Hair
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5500
Specialty
Physical Medicine

Promote hair growth in males with androgenic alopecia and norwood hamilton classification of iia to v

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More from Shenzhen Kaiyan Medical Equipment Co., Ltd.

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Questions and answers

When was LaserCap300, LaserCap224, LaserCap120, LaserCap80 cleared by the FDA?

LaserCap300, LaserCap224, LaserCap120, LaserCap80 (K161875) received a 510(k) decision of Substantially Equivalent on September 30, 2016, 84 days after the submission was received.

What is the product code of K161875?

The FDA product code is OAP – Laser, Comb, Hair, a Class II (moderate risk) device regulated under 21 CFR 890.5500.