FDA Device Intelligence
Home › WEERO Co., Ltd. › Apollo Quattro

Apollo Quattro

WEERO Co., Ltd. · Model APQ-10M · UDI-DI 08809851470114

PBXQPZIPFGZJIRT Prescription
2
510(k) clearances
63
Adverse events
1
Recalls
75
Facilities

Description

Apollo Quattro has a Q-EP handpiece, Q-LF handpiece, Q-FX handpiece, Q-SC handpiece, Q-BT handpiece, patch (cleared under K042301), patch cable, funnel hose, and power cable. The Q-LF, Q-FX, Q-SC, and Q-BT handpieces are used for radio frequency or low frequency output, while the Q-EP handpiece is used for heating or cooling output, or for low frequency when used with the patch and patch cable.

Recalls

DateFirmReason
2017-07-13Bios S.r.l.In some systems, the unit continues to emit RF energy after the PAUSE button is pressed.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.