# RF Medical Co., Ltd.

- Location (FDA's records): Seoul, KR
- FDA decisions: 4 (2018–2023): 4 510(k) clearances
- Product codes: GEI (4)
- 510(k) review time since 2016: median 181 days, against 105 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 3 (3 its own); citations of its devices by later devices: 3 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K180999: Mygen V-1000 RF System (2018), cited by 2
- K193355: Electrodes Handpieces for Mygen V-1000 RF System (2020), cited by 1

## Recent decisions
- K232763: Electrode Handpieces (VCT, RFTV, BMDT series) (Oct 4, 2023)
- K221277: Mygen M-3004 RF Generator M-3004 (Sep 2, 2022)
- K193355: Electrodes Handpieces for Mygen V-1000 RF System (Aug 3, 2020)
- K180999: Mygen V-1000 RF System (Dec 11, 2018)

Source page: https://510kreport.com/company/rf-medical