510(k) K062362 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
SINGLE USE ESOPHAGEAL MANOMETEY CATHETERS AND SINGLE USE ANO-RECTAL MANOMETRY CATHETERS
| Applicant | Sarmed Srl, Medolla, IT |
| Decision | Substantially Equivalent, Apr 13, 2007 |
| Received | Aug 14, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062362
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.