510(k) K971753 ยท DWM Apparatus, Suction, Patient Care
DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME DRAINAGE KIT, CATALOG NO. 50-7500
| Applicant | Denver Biomaterials, Inc., Golden CO, US |
| Decision | Unknown, Jun 27, 1997 |
| Received | May 12, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971753
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.