510(k) K882549 ยท FCG Biopsy Needle
ACUSON TRANSRECTAL NEEDLE GUIDE FOR INTRA. APPLI.
| Applicant | Acuson Corp., Mountain View CA, US |
| Decision | Substantially Equivalent, Jul 21, 1988 |
| Received | Jun 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882549
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.