510(k) K934391 ยท GYK Instrument, Shunt System Implantation
V/P AND L/P CATHETER PASSERS
| Applicant | Radionics, Inc., Burlington MA, US |
| Decision | Substantially Equivalent, Nov 19, 1993 |
| Received | Sep 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934391
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.