The following data is part of a premarket notification filed by Professional Medical Supply, Inc. with the FDA for Respi-neb-aerosol System.
| Device ID | K830417 |
| 510k Number | K830417 |
| Device Name: | RESPI-NEB-AEROSOL SYSTEM |
| Classification | Compressor, Air, Portable |
| Applicant | PROFESSIONAL MEDICAL SUPPLY, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BTI |
| CFR Regulation Number | 868.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-08 |
| Decision Date | 1983-03-24 |