510(k) K072131 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
M3 MONITOR
| Applicant | Spectrum Medical , Ltd., Gloucester, Gloucesterhsire, GB |
| Decision | Substantially Equivalent, Aug 17, 2007 |
| Received | Aug 2, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072131
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.