510(k) K770785 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
MONITOR, RESPIRATORY, TWO-GAS, RDC
| Applicant | Research Development Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, May 20, 1977 |
| Received | May 2, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770785
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.