510(k) K904417 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
CHEMOSITE IMPLANTABLE DRUG DELIVERY SYSTEM
| Applicant | Device Labs, Inc., Medway MA, US |
| Decision | Substantially Equivalent, Dec 5, 1990 |
| Received | Sep 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904417
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.