NEUROPACK MICRO, MODEL MED-9100A SERIES— 510(k) K010590
Substantially EquivalentNihon Kohden America, Inc.
FDA 510(k) clearance K010590 for NEUROPACK MICRO, MODEL MED-9100A SERIES, Substantially Equivalent on 2001-06-28. Applicant: Nihon Kohden America, Inc..
Clearance details
- Applicant
- Nihon Kohden America, Inc.
- Product code
- Code IKN
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Foothill, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.