K113845 is an FDA 510(k) clearance for the TUBING, CONMNECTORS, AND ACCESSORIES WIT BALANCE BIOSURFACE. This device is classified as a Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass (Class II - Special Controls, product code DTL).
Submitted by Medtronic, Inc. (Minneapolis, US). The FDA issued a Cleared decision on January 25, 2012, 28 days after receiving the submission on December 28, 2011.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.4290.
| 510(k) Number | K113845 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 28, 2011 |
| Decision Date | January 25, 2012 |
| Days to Decision | 28 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DTL — Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.4290 |