ASTRA 2,3,4 AND 6: CHIP REVISION
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Aug 19, 1986 |
| Received | Aug 8, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863000
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.