R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator
K-Number: K181688 · 2018-09-07
Device Summary
Frequently Asked Questions
What is the R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator?
R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator is a medical device that received FDA 510(k) clearance on 2018-09-07. It is manufactured by Shenzhen Roundwhale Technology Co. , Ltd.. The 510(k) number is K181688.
When was R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator approved by the FDA?
R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator received FDA 510(k) clearance on 2018-09-07, under approval number K181688.
What company makes R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator?
R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator is manufactured by Shenzhen Roundwhale Technology Co. , Ltd..
What is the FDA product code for R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator?
The FDA product code for R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator is IPF.
Other Devices by Shenzhen Roundwhale Technology Co. , Ltd.
Related Devices (Code: IPF)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.