510(k) K895725 ยท FCG Biopsy Needle
BIOPSY NEEDLE GUIDE FOR ADMS ULTRASOUND PROBES
| Applicant | Interson Corp., Pleasanton CA, US |
| Decision | Substantially Equivalent, Nov 6, 1989 |
| Received | Sep 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895725
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.