# K152587: DermaScalp Laser Cap

- Pathway: 510(k) (Traditional)
- Applicant: Dermascalp, LLC
- Decided: Feb 4, 2016 after 147 days
- Product code: OAP (Laser, Comb, Hair)
- Device class: 2
- Regulation: 21 CFR 890.5500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K001179 (2000). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150613: LaserCap LC Pro and LC Elite, Transdermal Cap, Inc. (2015) Summary page 4.

## Indications for use
The DermaScalp Laser Cap is indicated to promote hair growth in females with Androgenetic Alpopecia who have Ludwig-Savin Classifications I-II and who have Fitzpatrick Skin Types I to IV.

Source page: https://510kreport.com/device/K152587
Methodology: https://510kreport.com/methodology