510(k) K870016 ยท DTB Permanent Pacemaker Electrode
ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)
| Applicant | Migada, Ltd., Israel, IL |
| Decision | Substantially Equivalent, May 28, 1987 |
| Received | Jan 2, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870016
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.