ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000— 510(k) K863815
Substantially EquivalentElcot, Inc.
FDA 510(k) clearance K863815 for ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000, Substantially Equivalent on 1987-06-02. Applicant: Elcot, Inc..
Clearance details
- Applicant
- Elcot, Inc.
- Product code
- Code QGH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.