510(k) K833554 ยท DQO Catheter, Intravascular, Diagnostic
MATERIAL ADDITION LEXAN & K-RESIN
| Applicant | Procedure Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 12, 1984 |
| Received | Oct 5, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833554
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.