K151959 is an FDA 510(k) clearance for the AirLife Infant Single Limb Heated Wire Circuit. This device is classified as a Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer (Class II - Special Controls, product code BZE).
Submitted by Carefusion, Inc. (Vernon Hills, US). The FDA issued a Cleared decision on January 20, 2016, 188 days after receiving the submission on July 16, 2015.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5270.
| 510(k) Number | K151959 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 16, 2015 |
| Decision Date | January 20, 2016 |
| Days to Decision | 188 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | BZE - Heater, Breathing System W/wo Controller (not Humidifier Or Nebulizer |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5270 |