510(k) K900391 ยท BZG Spirometer, Diagnostic
FUKUDA DENSHI MODEL SPIROSIFT 3000
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Apr 10, 1990 |
| Received | Jan 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900391
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.