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FDA 510(k)

R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator

K-Number: K181688 · 2018-09-07

Decision Date2018-09-07
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator is a medical device manufactured by Shenzhen Roundwhale Technology Co. , Ltd.. It received FDA 510(k) clearance on 2018-09-07 under approval number K181688. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

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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.