# K892514: Ahrs Epilator 629

- Pathway: 510(k) (Traditional)
- Applicant: American Hair Removal System Co.
- Decided: Aug 14, 1990 after 490 days
- Product code: KCX (Epilator, High Frequency, Tweezer-Type)
- Device class: 1
- Regulation: 21 CFR 878.5360
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1,501 later devices descend from it; 2 cite it directly.
0 of 1,502 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K963249: Epilight Hair Removal System (1997), 1,499 descendants of its own
- K962446: Sharplan Ruby Laser System (1997), 1,497 descendants of its own
- K974536: Photoderm HR System (1998), 1,496 descendants of its own
- K991935: Epilight Hair Removal System, Photoderm HR System (2000), 1,492 descendants of its own
- K013366: Prolite Pulsed Light System for the Removal of Unwanted Hair (2002), 1,129 descendants of its own

Source page: https://510kreport.com/device/K892514
Methodology: https://510kreport.com/methodology