BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.— 510(k) K884852
Substantially EquivalentMoe
FDA 510(k) clearance K884852 for BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI., Substantially Equivalent on 1989-02-02. Applicant: Moe.
Clearance details
- Applicant
- Moe
- Product code
- Code HCC
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Soquel, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.