510(k) K924337 ยท GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
PLEUR-EVAC(R) ADULT/PEDI DUAL COLL CHEST DRAIN SYS
| Applicant | Deknatel, Inc., San Jose-Heredia, CR |
| Decision | Substantially Equivalent, Jul 28, 1993 |
| Received | Aug 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924337
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.