510(k) K922216 ยท KNT Tubes, Gastrointestinal (And Accessories)
FLEXIFLO TUBE PLACEMENT VERIFIER
| Applicant | Abbott Laboratories, Columbus OH, US |
| Decision | Substantially Equivalent, Jan 9, 1995 |
| Received | May 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922216
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.