510(k) K992173 ยท JXG Shunt, Central Nervous System And Components
SIPHONGUARD CSF CONTROL DEVICE
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Apr 7, 2000 |
| Received | Jun 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992173
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.