FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Capiox Advance Hardshell Reservoir
K Number: K153143
·
Decision Dec 2, 2015
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
168
Applicant Total
29
Review Days
33
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- Capiox Advance Hardshell Reservoir
- K Number
- K153143
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.4400
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Terumo Cardiovascular Systems Corporation
- Date Received
- October 30, 2015
- Decision Date
- December 2, 2015
- Product Code
- DTN
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DTN | Reservoir, Blood, Cardiopulmonary Bypass | FDA class 2 | Cardiovascular |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DTN), ordered by most recent decision date.
Inspire HCR and HCR DUAL cardiotomy reservoirs
FDA 510(k)
FDA Class 2
·Cardiovascular
Quantum Perfusion Hybrid System
FDA 510(k)
FDA Class 2
·Cardiovascular
MVR Venous Reservoir Bag 800 mL; MVR Venous Reservoir Bag 1600 mL; MVR Venous Reservoir Bag with Cortiva BioActive Surface 800 mL; MVR Venous Reservoir Bag with Cortiva BioActive Surface 1600 mL
FDA 510(k)
FDA Class 2
·Cardiovascular
BMR 1900 PHISIO
FDA 510(k)
FDA Class 2
·Cardiovascular
Intersept Filtered Cardiotomy Reservoir with Cortiva BioActive Surface
FDA 510(k)
FDA Class 2
·Cardiovascular
INSPIRE SVR 1200, INSPIRE 6F C, INSPIRE 8F C
FDA 510(k)
FDA Class 2
·Cardiovascular
Other Clearances by Terumo Cardiovascular Systems Corporation
| K Number | Device Name | ||
|---|---|---|---|
| K234065 | CDI OneView Monitoring System | Apr 25, 2024 | Substantially Equivalent |
| K221895 | Terumo Advanced Perfusion System 1 | Apr 18, 2023 | Substantially Equivalent |
| K200091 | Capiox iCP Centrifugal Pump | Nov 18, 2021 | Substantially Equivalent |
| K182110 | CDI Blood Parameter Monitoring System 550 | Nov 2, 2018 | Substantially Equivalent |
| K180950 | Terumo Capiox NX19 Oxygenator with Reservoir (east Orientation), Terumo Capiox NX19 Oxygenator with Reservoir (west Orientation), Terumo Capiox NX19 Oxygenator (east Orientation), Terumo Capiox NX19 Oxygenator (west Orientation) | Jun 22, 2018 | Substantially Equivalent |
| K172071 | Terumo Capiox NX19 Oxygenator with Reservoir (east orientation ), Terumo Capiox NX19 Oxygenator with Reservoir (west orientation ), Terumo Capiox NX19 Oxygenator (east orientation ), Terumo Capiox NX19 Oxygenator (west orientation) | Mar 29, 2018 | Substantially Equivalent |
| K172220 | Advanced Perfusion System 1 | Aug 17, 2017 | Substantially Equivalent |
| K163531 | Advanced Perfusion System 1 | Jun 7, 2017 | Substantially Equivalent |
| K162843 | Small (4) Roller Pump for the Terumo Advanced Perfusion System 1, Large (6) Roller Pump for the Terumo Advanced Perfusion System 1 | Nov 17, 2016 | Substantially Equivalent |
| K160206 | VirtuoSaph Plus Endoscopic Vessel Harvesting System | Apr 21, 2016 | Substantially Equivalent |