510(k) K871691 ยท KNT Tubes, Gastrointestinal (And Accessories)
MODIFIED MULTI-LUMEN NASOGASTRIC TUBE
| Applicant | Bissell Medical Products, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Aug 10, 1987 |
| Received | Apr 29, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871691
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.