510(k) K885220 ยท KNT Tubes, Gastrointestinal (And Accessories)
PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT
| Applicant | Ethox Corp., Buffalo NY, US |
| Decision | Unknown, Sep 25, 1989 |
| Received | Dec 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885220
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.