510(k) K881252 ยท GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
PLEUR-EVAC(R) A6000 ADULT/PEDIATRIC CHEST DRAINAGE
| Applicant | Deknatel, Inc., Lake Success NY, US |
| Decision | Substantially Equivalent, Jun 17, 1988 |
| Received | Mar 23, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881252
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.