K993194 is an FDA 510(k) clearance for the RUSCH MANUAL RESUSCITATOR BAG. This device is classified as a Ventilator, Emergency, Manual (resuscitator) (Class II - Special Controls, product code BTM).
Submitted by Rusch, Inc. (Duluth, US). The FDA issued a Cleared decision on March 24, 2000, 183 days after receiving the submission on September 23, 1999.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5915.
| 510(k) Number | K993194 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 23, 1999 |
| Decision Date | March 24, 2000 |
| Days to Decision | 183 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | BTM — Ventilator, Emergency, Manual (resuscitator) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5915 |