510(k) K854403 ยท BZG Spirometer, Diagnostic
MODEL 2120 SPIROSCREEN
| Applicant | Gould, Inc., Dayton OH, US |
| Decision | Substantially Equivalent, Jan 14, 1986 |
| Received | Oct 31, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854403
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.