The following data is part of a premarket notification filed by American Mcgaw with the FDA for Pab Iv Container.
| Device ID | K840388 |
| 510k Number | K840388 |
| Device Name: | PAB IV CONTAINER |
| Classification | Container, I.v. |
| Applicant | AMERICAN MCGAW 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPE |
| CFR Regulation Number | 880.5025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-01-30 |
| Decision Date | 1984-03-06 |