510(k) K151932 ยท HRX Arthroscope
Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing
| Applicant | Stryker Corporation, San Jose CA, US |
| Decision | Substantially Equivalent, Mar 31, 2016 |
| Received | Jul 14, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151932
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.