510(k) K923028 ยท GCB Needle, Catheter
TURKEL PNEUMOTHORAX KIT
| Applicant | Symbiosis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Aug 4, 1992 |
| Received | Jun 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923028
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.