510(k) K865075 ยท GYK Instrument, Shunt System Implantation
H-H SUBGALEAL TROCAR
| Applicant | Holter-Hausner Intl., Bridgeport PA, US |
| Decision | Substantially Equivalent, Jan 13, 1987 |
| Received | Dec 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K865075
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.