The following data is part of a premarket notification filed by Medical Industries America, Inc. with the FDA for 3000 Aerosol Two.
| Device ID | K943990 |
| 510k Number | K943990 |
| Device Name: | 3000 AEROSOL TWO |
| Classification | Nebulizer (direct Patient Interface) |
| Applicant | MEDICAL INDUSTRIES AMERICA, INC. 2879 R AVE. Adel, IA 50003 -8055 |
| Contact | Mark D Hebensteit |
| Correspondent | Mark D Hebensteit MEDICAL INDUSTRIES AMERICA, INC. 2879 R AVE. Adel, IA 50003 -8055 |
| Product Code | CAF |
| CFR Regulation Number | 868.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-16 |
| Decision Date | 1995-03-21 |