INTERFLO MEDICAL MODEL F-1 THERMODILUTION CATHETER— 510(k) K900710
Substantially EquivalentIntec Medical, Inc.
FDA 510(k) clearance K900710 for INTERFLO MEDICAL MODEL F-1 THERMODILUTION CATHETER, Substantially Equivalent on 1990-10-19. Applicant: Intec Medical, Inc..
Clearance details
- Applicant
- Intec Medical, Inc.
- Product code
- Code KRB
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plano, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.