510(k) K905018 ยท DQO Catheter, Intravascular, Diagnostic
LAB-SITE SAFETY NEEDLE
| Applicant | Telos Medical Corp., Keene CA, US |
| Decision | Substantially Equivalent, Jan 16, 1991 |
| Received | Nov 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905018
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.