510(k) K970372 ยท FDF Colonoscope And Accessories, Flexible/Rigid
GASTROSCOPE AND COLONOSCOPE NOZZLE REPLACEMENT KITS
| Applicant | Precision Endoscopy of America, Inc., Hunt Valley MD, US |
| Decision | Substantially Equivalent, Mar 11, 1997 |
| Received | Jan 31, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970372
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.