The following data is part of a premarket notification filed by Airlife, Inc. with the FDA for Manifold, Universal I.p.p.b.
| Device ID | K790152 |
| 510k Number | K790152 |
| Device Name: | MANIFOLD, UNIVERSAL I.P.P.B |
| Classification | Nebulizer (direct Patient Interface) |
| Applicant | AIRLIFE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CAF |
| CFR Regulation Number | 868.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-01-12 |
| Decision Date | 1979-03-07 |