510(k) K932273 ยท GYK Instrument, Shunt System Implantation
CORDIS TUNNELER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Aug 23, 1993 |
| Received | May 13, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932273
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.