510(k) K992101 ยท CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
CRITERION 40 OR PM 40
| Applicant | Caradyne, Ltd., Mccordsville IN, US |
| Decision | Substantially Equivalent, Jan 6, 2000 |
| Received | Jun 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992101
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.