The following data is part of a premarket notification filed by Airlife, Inc. with the FDA for Air Incentive Spirometer, W/nebulizer.
| Device ID | K792217 |
| 510k Number | K792217 |
| Device Name: | AIR INCENTIVE SPIROMETER, W/NEBULIZER |
| Classification | Spirometer, Therapeutic (incentive) |
| Applicant | AIRLIFE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BWF |
| CFR Regulation Number | 868.5690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-05 |
| Decision Date | 1979-11-27 |