MYOMETER EMG BIOFEEDBACK DEVICE— 510(k) K850849
Substantially EquivalentPhysio Technology, Inc.
FDA 510(k) clearance K850849 for MYOMETER EMG BIOFEEDBACK DEVICE, Substantially Equivalent on 1985-05-31. Applicant: Physio Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- Physio Technology, Inc.
- Product code
- Code HCC
- Device class
- Class 2
- Regulation
- 21 CFR 882.5050
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Topeka, KS, US
Recent devices under product code HCC
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