# K213078: Myolift QT

- Pathway: 510(k) (Traditional)
- Applicant: Johari Digital Healthcare Limited
- Decided: Apr 27, 2023 after 581 days
- Product code: NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes)
- Device class: 2
- Regulation: 21 CFR 882.5890
- 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 K011935 (2001). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K212342: ZIIP+ Device, Ziip, Inc. (2021) Summary page 5.

## Indications for use
“Myolift QT” is indicated for facial and neck stimulation and is indicated for over-the-counter cosmetic use.

Source page: https://510kreport.com/device/K213078
Methodology: https://510kreport.com/methodology