BIOFEEDBACK DEVICE TG3, TG4— 510(k) K884851
Substantially EquivalentMoe
FDA 510(k) clearance K884851 for BIOFEEDBACK DEVICE TG3, TG4, Substantially Equivalent on 1989-02-03. 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.