# K973773: Dapelle Hair Remover

- Pathway: 510(k) (Traditional)
- Applicant: Wellquest Intl., Inc.
- Decided: Dec 17, 1997 after 76 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Intended use for this product is to remove unwanted hair.

Source page: https://510kreport.com/device/K973773
Methodology: https://510kreport.com/methodology