The following data is part of a premarket notification filed by James L. Geraci & Associates, Inc. with the FDA for Airmed Pneumatic Equip. Filtra/control.
| Device ID | K820079 |
| 510k Number | K820079 |
| Device Name: | AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL |
| Classification | Compressor, Air, Portable |
| Applicant | JAMES L. GERACI & ASSOCIATES, 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 | 1982-01-12 |
| Decision Date | 1982-02-05 |