# K150578: Capillus 272 Office Pro

- Pathway: 510(k) (Traditional)
- Applicant: Capillus, LLC
- Decided: Jun 9, 2015 after 92 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: 1 generation back to K143199 (2015). 1 ancestor in all.
4 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143199: Capillus 272 Pro, Capillus, LLC (2015) Summary page 5.
- (no number) iGrow II Hair Growth System: named in the summary without a submission number
- (no number) Sunetics Clinical Laser “G” or “W2326”: named in the summary without a submission number

## Most influential descendants
- K192585: Bosley Revitalizer 96 Laser Cap, Bosley Revitalizer 96 XL Laser Cap (2020), 3 descendants of its own
- K240456: Bosley Booster 128 Laser Cap; Bosley Booster 162 Laser Cap; Bosley Booster 288 Laser Cap (2024), 2 descendants of its own
- K261675: CHZL Red Light Therapy Hair Growth Cap (Model (s):CHZL-120BK-L52D,CHZL-120BK-L53D,CHZL-120BK-L54D) (2026), 0 descendants of its own
- K251017: CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A) (2025), 0 descendants of its own

## Indications for use
Promote hair growth in females diagnosed with androgenetic alopecia presenting with Ludwig-Savin Classifications I-11 and Fitzpatrick Skin Phototypes I-IV.

Source page: https://510kreport.com/device/K150578
Methodology: https://510kreport.com/methodology