510(k) K013705 ยท GWM Device, Monitoring, Intracranial Pressure
ACT III VENTRICULAR CATHETER
| Applicant | Innerspace, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Sep 9, 2002 |
| Received | Nov 8, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013705
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.