The following data is part of a premarket notification filed by Manuco Manufacturing Co., Inc. with the FDA for Magun Base I.v. Pole.
| Device ID | K821405 |
| 510k Number | K821405 |
| Device Name: | MAGUN BASE I.V. POLE |
| Classification | Stand, Infusion |
| Applicant | MANUCO MANUFACTURING CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FOX |
| CFR Regulation Number | 880.6990 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-11 |
| Decision Date | 1982-06-16 |