510(k) K992907 ยท GBW Catheter, Peritoneal
INTRADUCER
| Applicant | Taut, Inc., Geneva IL, US |
| Decision | Substantially Equivalent, Oct 5, 1999 |
| Received | Aug 30, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992907
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 14, 2015 | Teleflex Medical Taut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93. To provide an access port into the peritoneal cavity. Terminated |
GBW | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.