510(k) K882551 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
AMBULATORY PH DATA RECORDER SYSTEM, APH-2000
| Applicant | Intl. Biomedics, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Oct 12, 1988 |
| Received | Jun 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882551
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.