# K973340: Tweezer-Type Epilator

- Pathway: 510(k) (Traditional)
- Applicant: Mobit, Inc.
- Decided: Dec 3, 1997 after 89 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 sole indication for use of this medical device is as an epilator for the removal of undesired body hairs using the techniques described in the Owner’s Instruction Brochure.

Source page: https://510kreport.com/device/K973340
Methodology: https://510kreport.com/methodology