510(k) K930568 ยท GCB Needle, Catheter
ADAIR/VERESS NEEDLE INTRODUCER SET
| Applicant | Medical Dynamics, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Jul 22, 1993 |
| Received | Jan 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930568
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.