510(k) K990321 ยท MNR Ventilatory Effort Recorder
ALPHAMED GEMINI SENSOR, SNORING SENSOR
| Applicant | Alphamed, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 1, 1999 |
| Received | Feb 1, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990321
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.