510(k) K882286 ยท GWM Device, Monitoring, Intracranial Pressure
EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET
| Applicant | Metatech Corp., Wheeling IL, US |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | Jun 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882286
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.