Hair Growth Comb (SZ-23,SZ-23A)

FDA 510(k) K241342 · Shenzhen Nuon Medical Equipment Co., Ltd.

Substantially Equivalent

510(k) numberK241342

Submission

Device name
Hair Growth Comb (SZ-23,SZ-23A)
Applicant
Shenzhen Nuon Medical Equipment Co., Ltd.
Shenzhen, CN
Received
May 13, 2024
Decision date
November 8, 2024
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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Questions and answers

When was Hair Growth Comb (SZ-23,SZ-23A) cleared by the FDA?

Hair Growth Comb (SZ-23,SZ-23A) (K241342) received a 510(k) decision of Substantially Equivalent on November 8, 2024, 179 days after the submission was received.

What is the product code of K241342?

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