510(k) K141793 ยท BZG Spirometer, Diagnostic
PULMONE MINIBOXPFT 2.0
| Applicant | Pulmone Advanced Medical Devices, Ltd., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 6, 2015 |
| Received | Jul 2, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141793
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.