CAPIOX FX HOLLOW FIBER OXYGENATOR W/ RESERVOIR— 510(k) K130280
Substantially EquivalentTerumo Corporation
FDA 510(k) clearance K130280 for CAPIOX FX HOLLOW FIBER OXYGENATOR W/ RESERVOIR, Substantially Equivalent on 2013-03-13. Applicant: Terumo Corporation. Device class: 2.
Clearance details
- Applicant
- Terumo Corporation
- Product code
- Code DTZ
- Device class
- Class 2
- Regulation
- 21 CFR 870.4350
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Elkton, MD, US
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More clearances from Terumo Corporation
view allAdverse events under product code DTZ
product code DTZ- Death
- 182
- Injury
- 422
- Malfunction
- 3,636
- Total
- 4,240
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.