510(k) K780894 ยท BZG Spirometer, Diagnostic
AIRFLOMETER
| Applicant | Glaxo Australia Ply. , Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 14, 1978 |
| Received | May 26, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780894
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.