FDA 510(k) Applications Submitted by Shenzhen Roundwhale Technology Co. Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K231423 05/17/2023 Combo Electrotherapy Device (Models: R-C101C, R-C101D, R-C101F, R-C101G, F100, MINI-TENS-COMB, RC101I, TENS3500) Shenzhen Roundwhale Technology Co. Ltd.


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