VITAPORT 3— 510(k) K000338
Substantially EquivalentNihon Kohden America, Inc.
FDA 510(k) clearance K000338 for VITAPORT 3, Substantially Equivalent on 2000-04-26. Applicant: Nihon Kohden America, Inc..
Clearance details
- Applicant
- Nihon Kohden America, Inc.
- Product code
- Code OLV
- Advisory panel
- Neurology
- 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.