510(k) K883158 ยท BZQ Monitor, Breathing Frequency
RESPIRATORY AIRWAY TUBE MONITOR (RATM)
| Applicant | Vascucare, Inc., Orangeburg NY, US |
| Decision | Substantially Equivalent, Mar 6, 1989 |
| Received | Jul 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883158
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.