510(k) K873441 ยท KNT Tubes, Gastrointestinal (And Accessories)
BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBE
| Applicant | Bissell Medical Products, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Oct 27, 1987 |
| Received | Aug 27, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873441
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.