The following data is part of a premarket notification filed by Medical Industries America, Inc. with the FDA for Maxi Compressors.
| Device ID | K900686 |
| 510k Number | K900686 |
| Device Name: | MAXI COMPRESSORS |
| Classification | Compressor, Air, Portable |
| Applicant | MEDICAL INDUSTRIES AMERICA, INC. 2875 R AVE. Adel, IA 50003 |
| Contact | Russell F Bird |
| Correspondent | Russell F Bird MEDICAL INDUSTRIES AMERICA, INC. 2875 R AVE. Adel, IA 50003 |
| Product Code | BTI |
| CFR Regulation Number | 868.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-02-13 |
| Decision Date | 1990-04-26 |