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.. Device class: 2.
Clearance details
- Applicant
- Intec Medical, Inc.
- Product code
- Code KRB
- Device class
- Class 2
- Regulation
- 21 CFR 870.1915
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plano, TX, US
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More clearances from Intec Medical, Inc.
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