Stryker Corporation · Class II · Cleared Mar 31, 2016
| K-number | K151932 |
| Device name | Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing |
| Applicant | Stryker Corporation |
| Product code | HRX |
| Device class | Class II |
| Decision date | Mar 31, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 888.1100 |
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