510(k) K020301 ยท FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology
MODIFICATION TO VISTA STEREOSCOPE SYSTEM
| Applicant | Vista Medical Technologies, Inc., Westborough MA, US |
| Decision | Substantially Equivalent, Feb 12, 2002 |
| Received | Jan 29, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020301
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.