Grivamax Hair Growth System

FDA 510(k) K171895 · Leana Orders, Inc.

Substantially Equivalent

510(k) numberK171895

Submission

Device name
Grivamax Hair Growth System
Applicant
Leana Orders, Inc.
Staten Island, NY, US
Received
June 26, 2017
Decision date
August 22, 2017
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 Grivamax Hair Growth System cleared by the FDA?

Grivamax Hair Growth System (K171895) received a 510(k) decision of Substantially Equivalent on August 22, 2017, 57 days after the submission was received.

What is the product code of K171895?

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