510(k) K081889 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
RHAPSODY CT
| Applicant | Grantadler Corporation, Appollo Beach FL, US |
| Decision | Substantially Equivalent, Nov 12, 2008 |
| Received | Jul 2, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081889
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.