NIHON KOHDEN ECG-9320A CARDIOFAX AND ACCESSORIES— 510(k) K961272
Substantially EquivalentNihon Kohden America, Inc.
FDA 510(k) clearance K961272 for NIHON KOHDEN ECG-9320A CARDIOFAX AND ACCESSORIES, Substantially Equivalent on 1996-11-01. Applicant: Nihon Kohden America, Inc..
Clearance details
- Applicant
- Nihon Kohden America, Inc.
- Product code
- Code LOS
- Advisory panel
- Unknown
- 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.