510(k) K900569 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
THERMOPROBE 210
| Applicant | Merced Medical, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Apr 10, 1990 |
| Received | Feb 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900569
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.