510(k) K934640 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
HMP DUAL POLYSULFONE PORT
| Applicant | Horizon Medical Products, Inc., Atlanta GA, US |
| Decision | Unknown, Feb 25, 1994 |
| Received | Sep 28, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934640
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.