510(k) K882383 ยท DWZ Device, Biopsy, Endomyocardial
MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES
| Applicant | CIVCO Medical Instruments Co., Inc., Kalona IA, US |
| Decision | Substantially Equivalent, Nov 28, 1988 |
| Received | Jun 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882383
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.