510(k) K790304 ยท BZQ Monitor, Breathing Frequency
PREAMPLIFIER MODULE, EKG RESPIRATION
| Applicant | Abbott Medical Electronics Co., Fort Worth TX, US |
| Decision | Substantially Equivalent, Feb 27, 1979 |
| Received | Feb 13, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790304
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.