Sanyo Electronic Muscle Stimulators
FDA 510(k) K850047 · General Physiotherapy, Inc.
510(k) numberK850047
Submission
- Device name
- Sanyo Electronic Muscle Stimulators
- Applicant
- General Physiotherapy, Inc.
St. Louis, MO, US - Received
- January 8, 1985
- Decision date
- March 5, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- IPF – Stimulator, Muscle, Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.5850
- Specialty
- Physical Medicine
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|---|---|---|---|
| K253542 | Apollo Quattro (APQ-10M)IPF · Traditional | Weero Co., Ltd. | 06/08/2026SE |
| K252816 | High Tone Power therapy (HiToP) (Model: HiToP PNP)IPF · Traditional | Mohammadali Nezakati | 06/02/2026SE |
| K260142 | StimelMD (SSMD) systemIPF · Special | Motion Informatics ltd. | 05/27/2026SE |
| K251083 | Compact IIIPF · Traditional | Enraf-Nonius, B.V. | 09/12/2025SE |
| K241433 | EVE Synergy (EVE-20M)IPF · Traditional | Weero Co., Ltd. | 06/04/2025SE |
| K241488 | TrainFES AdvanceIPF · Traditional | Trainfes | 02/05/2025SE |
| K240348 | Quantum Mitohormesis (QMT) (M2101)IPF · Abbreviated | Quantumtx Pte. , Ltd. | 12/19/2024SE |
| K240992 | eMVFit (MVF-10M)IPF · Traditional | Weero Co., Ltd. | 10/10/2024SE |
| K240234 | BTL-899MSIPF · Traditional | BTL Industries, Inc. | 08/17/2024SE |
| K233098 | MYOTouch Muscle StimulatorIPF · Traditional | Sunmed, LLC | 08/02/2024SE |
More from Sunmed, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K870939 | VibracareISA · Traditional | 04/06/1987SE |
| K863383 | Facial Massager, Battery PoweredISA · Traditional | 09/15/1986SE |
| K861834 | Theracushion Model 1000ISA · Traditional | 05/27/1986SE |
| K855129 | Neocussor (Massager, Battery) PoweredBYI · Traditional | 01/23/1986SE |
| K853710 | TheracushionISA · Traditional | 01/03/1986SE |
| K852944 | Fleximatic MassagerISA · Traditional | 09/05/1985SE |
| K844591 | Mist-Ease NebulizerCCQ · Traditional | 12/13/1984SE |
| K810244 | Porta-Puls Muscle StimulatorIRO · Traditional | 02/26/1981SE |
Questions and answers
When was Sanyo Electronic Muscle Stimulators cleared by the FDA?
Sanyo Electronic Muscle Stimulators (K850047) received a 510(k) decision of Substantially Equivalent on March 5, 1985, 56 days after the submission was received.
What is the product code of K850047?
The FDA product code is IPF – Stimulator, Muscle, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.5850.