The following data is part of a premarket notification filed by Airlife, Inc. with the FDA for Volume Ventilator Circuit-nebulizer.
| Device ID | K833196 |
| 510k Number | K833196 |
| Device Name: | VOLUME VENTILATOR CIRCUIT-NEBULIZER |
| Classification | Circuit, Breathing (w Connector, Adaptor, Y Piece) |
| Applicant | AIRLIFE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CAI |
| CFR Regulation Number | 868.5240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-19 |
| Decision Date | 1983-11-03 |