510(k) K022023 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500
| Applicant | Clinical Innovations, Inc., Murray UT, US |
| Decision | Substantially Equivalent, Jan 7, 2003 |
| Received | Jun 20, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022023
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.