510(k) K022248 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems
STRYKER L3 HYDROLERT
| Applicant | Stryker Endoscopy, San Jose CA, US |
| Decision | Substantially Equivalent, Aug 6, 2002 |
| Received | Jul 12, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022248
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.