510(k) K961972 ยท BZQ Monitor, Breathing Frequency
MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR
| Applicant | Aequitron Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Apr 18, 1997 |
| Received | May 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961972
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.