510(k) K882223 ยท KDQ Bottle, Collection, Vacuum
PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST
| Applicant | Deknatel, Inc., Lake Success NY, US |
| Decision | Substantially Equivalent, Aug 16, 1988 |
| Received | May 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882223
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.