510(k) K974096 ยท JXG Shunt, Central Nervous System And Components
CRX DIAMOND VALVE
| Applicant | Phoenix Biomedical Corp., Norristown PA, US |
| Decision | Substantially Equivalent, Dec 8, 1998 |
| Received | Oct 30, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974096
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.