The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Chest Bellows, Small.
| Device ID | K772367 |
| 510k Number | K772367 |
| Device Name: | CHEST BELLOWS, SMALL |
| Classification | Plethysmograph, Pressure |
| Applicant | HONEYWELL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CCM |
| CFR Regulation Number | 868.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-12-27 |
| Decision Date | 1978-01-11 |