510(k) K890431 ยท GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
PLEUR-EVAC(R) A-8000--ADULT/PEDIATRIC CHEST DRAIN
| Applicant | Deknatel, Inc., San Jose-Heredia, CR |
| Decision | Substantially Equivalent, Apr 4, 1989 |
| Received | Jan 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890431
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.