K220854 is an FDA 510(k) clearance for the TrachCuff Cuff Controller. This device is classified as a Cuff, Tracheal Tube, Inflatable (Class II - Special Controls, product code BSK).
Submitted by Aw Technologies Aps (Norresundby, DK). The FDA issued a Cleared decision on April 14, 2023, 387 days after receiving the submission on March 23, 2022.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5750.
| 510(k) Number | K220854 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 23, 2022 |
| Decision Date | April 14, 2023 |
| Days to Decision | 387 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | BSK - Cuff, Tracheal Tube, Inflatable |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5750 |