MEB-5200— 510(k) K854664
Substantially EquivalentNihon Kohden America, Inc.
FDA 510(k) clearance K854664 for MEB-5200, Substantially Equivalent on 1986-08-14. Applicant: Nihon Kohden America, Inc..
Clearance details
- Applicant
- Nihon Kohden America, Inc.
- Product code
- Code IKT
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.