510(k) K820269 ยท DWO Needle, Biopsy, Cardiovascular
RNG SERIES ULTRASOUND NEEDLE/CATH. GDS
| Applicant | CIVCO Medical Instruments Co., Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 23, 1982 |
| Received | Feb 2, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820269
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.