510(k) K011283 ยท NGT Saline, Vascular Access Flush
MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE
| Applicant | The Kendall Company, Mansfield MA, US |
| Decision | Substantially Equivalent, Oct 15, 2001 |
| Received | Apr 27, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011283
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.