510(k) K900754 ยท BWF Spirometer, Therapeutic (Incentive)
RESPIREX 2
| Applicant | Diemolding Corp., Canastota NY, US |
| Decision | Substantially Equivalent, Mar 15, 1990 |
| Received | Feb 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900754
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.