The following data is part of a premarket notification filed by Medix Of Florida, Inc. with the FDA for Traveler Nebulizing System.
| Device ID | K832220 |
| 510k Number | K832220 |
| Device Name: | TRAVELER NEBULIZING SYSTEM |
| Classification | Compressor, Air, Portable |
| Applicant | MEDIX OF FLORIDA, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | BTI |
| CFR Regulation Number | 868.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-07-08 |
| Decision Date | 1983-09-26 |