# Shenzhen RF Tech Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 12 (2015–2026): 12 510(k) clearances
- Product codes: MOS (11), LNH (1)
- 510(k) review time since 2016: median 123 days, against 51 for FDA's reviews in the same codes and years (1 of 11 faster)
- Predicates its devices cite: 12 (4 its own); citations of its devices by later devices: 4 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mri Devices Corp.: 3 (https://510kreport.com/company/mri-devices)
- Neocoil, LLC: 3 (https://510kreport.com/company/neocoil)
- Ge Hangwei Medical Systems Co., Ltd.: 2 (https://510kreport.com/company/ge-hangwei-medical-systems)

## Its most-cited devices
- K223225: 8ch T/R Knee Coil (2023), cited by 1
- K172222: 8ch Flex Suite (2017), cited by 1
- K223239: 8ch Wrist Coil (2022), cited by 1
- K151653: 8ch Foot Ankle Coil (2015), cited by 1

## Recent decisions
- K252587: HD 8Ch Wrist Array (Apr 14, 2026)
- K252876: GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive Only (Apr 1, 2026)
- K252179: GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive Only; GEM Flex Coil 16-S Array, 1.5T Receive Only (Feb 10, 2026)
- K231085: 1.5T HD T/R Knee Array (10-F34127) (Aug 18, 2023)
- K223203: 1.5T 24E Posterior Array (Mar 2, 2023)
- K223225: 8ch T/R Knee Coil (Feb 14, 2023)
- K223239: 8ch Wrist Coil (Dec 8, 2022)
- K200836: 8ch Flex Suite (Jul 22, 2020)

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