# K253261: Apollo Quattro (APQ-10M)

- Pathway: 510(k) (Traditional)
- Applicant: Weero Co., Ltd.
- Decided: Mar 13, 2026 after 165 days
- Product code: PBX (Massager, Vacuum, Radio Frequency Induced Heat)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K010991 (2001). 77 ancestors in all.
No later device cites it as a predicate yet.
0 of 78 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K212253: Apollo Duet (Model : APD-4000), Weero Co. (2022) Summary page 5.
- K213294: Dermal Cooling System, R2 Technologies, Inc. (2022) Summary page 5.

## Indications for use
Q-LF handpiece, Q-FX handpiece, Q-SC handpiece, and Q-BT handpiece in RF mode are intended for: Relief of minor muscle aches and pain, relief of muscle spasm, and temporary improvement of local blood circulation. Q-EP handpiece in cooling mode is intended for: Use in dermatologic procedures for the removal of benign lesions of the skin and for the temporary reduction of pain, swelling, inflammation, and hematoma from minor surgical procedures.

Source page: https://510kreport.com/device/K253261
Methodology: https://510kreport.com/methodology