510(k) K033939 ยท BZG Spirometer, Diagnostic
FLOSENSE II, MODEL 29-8040
| Applicant | Sdi Diagnostics, Inc., Easton MA, US |
| Decision | Substantially Equivalent, Jan 30, 2004 |
| Received | Dec 15, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033939
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.