ELEKIBAN MAGNETO-THERAPEUTIC DEVICE— 510(k) K850172
Substantially EquivalentMns, Ltd.
FDA 510(k) clearance K850172 for ELEKIBAN MAGNETO-THERAPEUTIC DEVICE, Substantially Equivalent on 1985-04-16. Applicant: Mns, Ltd..
Clearance details
- Applicant
- Mns, Ltd.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.