510(k) K881402 ยท BZG Spirometer, Diagnostic
629V SPIROMETER, PULMONARY FUNCTION ANALYZER
| Applicant | American Electromedics Corp., Hudson NH, US |
| Decision | Substantially Equivalent, Sep 26, 1988 |
| Received | Apr 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881402
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.