CAPIOX E HOLLOW FIBER OXYGENATOR WITH INTEGRATED HEAT EXCHANGER/ARTERIAL RESERVOIR
FDA 510(k) clearance K970463 · decided 1997-05-06
Clearance details
- K-number
- K970463
- Device name
- CAPIOX E HOLLOW FIBER OXYGENATOR WITH INTEGRATED HEAT EXCHANGER/ARTERIAL RESERVOIR
- Applicant
- Terumo Medical Corp.
- Decision
- Substantially Equivalent
- Date received
- 1997-02-06
- Decision date
- 1997-05-06
- Days to decision
- 89 days
- Clearance type
- Traditional
- Product code
- DTZ
- Device class
- 2
- Regulation number
- 870.4350
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Elkton, MD, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.