EMG BIOFEEDBACK DEVICE— 510(k) K823511
Substantially EquivalentNemectron Medical, Inc.
FDA 510(k) clearance K823511 for EMG BIOFEEDBACK DEVICE, Substantially Equivalent on 1983-03-31. Applicant: Nemectron Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Nemectron Medical, 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
- Walker, MI, US
Recent devices under product code HCC
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