Shenzhen Roundwhale Technology Co. , Ltd.
FDA 510(k) medical device clearances.
Top product codes for Shenzhen Roundwhale Technology Co. , Ltd.
Recent clearances by Shenzhen Roundwhale Technology Co. , Ltd.
- K231423 — Combo Electrotherapy Device (Models: R-C101C, R-C101D, R-C101F, R-C101G, F100, MINI-TENS-COMB, RC101I, TENS3500)
- K232995 — Neurological Therapy Devices - Accessories: Electrotherapy device Electrode belt for Abdominal Muscle Trainer Toning, AC1001, AC1002, AC1003, AC1003, AC1004, AC1005; Electrotherapy device Electrode belt for back of body, AC2001, AC2002, AC2003, AC2004; Electrotherapy device Electrode belt for Body joints, AC3001, AC3008, AC3009, AC3010, AC3011; Electrotherapy device Electrode for Knee, AC3002, AC3004, AC3006; Electrotherapy device Electrode for Elbow, AC3003, AC3005, AC3007; Electrothe
- K231440 — Combo Electrotherapy Device
- K222252 — Self-adhesive Electrode
- K192087 — Combo Electrotherapy Device
- K181688 — R-C1 TENS and EMS Stimulator; R-E1- EMS Stimulator; R-T1 TENS Stimulator
- K180956 — Electrical Stimulator - Model R-C1 TENS and EMS stimulator, Model R-E1 EMS stimulator, Model R-T1 TENS Stimulator
Data sourced from openFDA. This site is unofficial and independent of the FDA.