510(k) K833433 ยท DQY Catheter, Percutaneous
PHYSIO-PROBE-HIGH PERMEABILITY CATH.
| Applicant | Research Industries Corp., Walker MI, US |
| Decision | Substantially Equivalent, Dec 29, 1983 |
| Received | Oct 5, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833433
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.