K811404 is an FDA 510(k) clearance for the TRAVELAIRE. This device is classified as a Nebulizer, Medicinal, Non-ventilatory (atomizer) (Class I - General Controls, product code CCQ).
Submitted by B & F Medical Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 9, 1981, 22 days after receiving the submission on May 18, 1981.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5640.
| 510(k) Number | K811404 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 18, 1981 |
| Decision Date | June 09, 1981 |
| Days to Decision | 22 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CCQ — Nebulizer, Medicinal, Non-ventilatory (atomizer) |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 868.5640 |