510(k) K991222 ยท GWM Device, Monitoring, Intracranial Pressure
CODMAN MICROSENSOR VENTRICULAR CATHETER KIT
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Jul 9, 1999 |
| Received | Apr 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991222
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.