K992530 is an FDA 510(k) clearance for the BIPAP SYNCHRONY HC. This device is classified as a Ventilator, Continuous, Non-life-supporting (Class II - Special Controls, product code MNS).
Submitted by Respironics, Inc. (Murrysville, US). The FDA issued a Cleared decision on March 20, 2000, 236 days after receiving the submission on July 28, 1999.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5895.
| 510(k) Number | K992530 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 28, 1999 |
| Decision Date | March 20, 2000 |
| Days to Decision | 236 days |
| Submission Type | Abbreviated |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | MNS — Ventilator, Continuous, Non-life-supporting |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5895 |