510(k) K800419 ยท FCG Biopsy Needle
ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOL
| Applicant | A.D.T. Lab Industries, Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 25, 1980 |
| Received | Feb 26, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800419
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.