510(k) K032888 ยท DQO Catheter, Intravascular, Diagnostic
CREATION NM DIAGNOSTIC CATHETERS
| Applicant | Neich Medical (Shenzhen) Company Limited, Shenzhen, CN |
| Decision | Substantially Equivalent, Feb 24, 2004 |
| Received | Sep 16, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032888
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.