INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETER
FDA 510(k) clearance K911840 · decided 1991-06-03
Clearance details
- K-number
- K911840
- Device name
- INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETER
- Applicant
- Intec Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-04-25
- Decision date
- 1991-06-03
- Days to decision
- 39 days
- Clearance type
- Traditional
- Product code
- DYG
- Device class
- 2
- Regulation number
- 870.1240
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Arlington, VA, US
- Third-party review
- No
- Expedited review
- No
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| Swang-Ganz IQ pulmonary artery catheter (K222117) | Edwards Lifesiences, LLC | 2022-12-09 |
| Swan-Ganz Catheters (K193466) | Edwards Lifesciences, LLC | 2020-02-16 |
| Swan Ganz Catheters (K160084) | Edwards Lifesciences, LLC | 2016-05-03 |
| PERCUPRO MESSENGER BALLOON CATHETER (K094048) | Cardiosolutions, Inc. | 2011-07-14 |
| OCCLUSION BALLOON CATHETER, MODEL VENOS (K081052) | Oscor, Inc. | 2008-06-18 |
| ANGIO FLOW THERMODILUTION CATHETER, MODEL AF-CATH-01; ANGIOFLOW METER, MODELS HQ100 AND HQ101 (K010253) | Transonic Systems, Inc. | 2002-03-19 |
| ATTAIN 6215 VENOGRAM BALLOON CATHETER (K012225) | Medtronic Vascular | 2001-08-28 |
| Z2 BALLOON GUIDED PACING & PRESSURE MONITORING CATHETER, MODEL Z2-7-02-1-10-0 (K003118) | Zcv ,Inc. | 2000-12-20 |
Recalls involving this device
No recalls on record reference this clearance.