iHelmet Hair Growth System

FDA 510(k) K190467 · Slinph Technologies Co., Ltd.

Substantially Equivalent

510(k) numberK190467

Submission

Device name
iHelmet Hair Growth System
Applicant
Slinph Technologies Co., Ltd.
Shenzhen, CN
Received
February 26, 2019
Decision date
December 26, 2019
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 iHelmet Hair Growth System cleared by the FDA?

iHelmet Hair Growth System (K190467) received a 510(k) decision of Substantially Equivalent on December 26, 2019, 303 days after the submission was received.

What is the product code of K190467?

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