510(k) K242110 ยท FDF Colonoscope And Accessories, Flexible/Rigid
PENTAX Medical Video Colonoscope (EC38-i20cWL)
| Applicant | Pentax of America, Inc., Montvale NJ, US |
| Decision | Substantially Equivalent, Jan 3, 2025 |
| Received | Jul 19, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242110
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.