The following data is part of a premarket notification filed by Plasco, Inc. with the FDA for Pharmafeed.
| Device ID | K932649 |
| 510k Number | K932649 |
| Device Name: | PHARMAFEED |
| Classification | Container, I.v. |
| Applicant | PLASCO, INC. 3849 SWANSON ST. Gurnee, IL 60031 -1225 |
| Contact | Gary S Botsford |
| Correspondent | Gary S Botsford PLASCO, INC. 3849 SWANSON ST. Gurnee, IL 60031 -1225 |
| Product Code | KPE |
| CFR Regulation Number | 880.5025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-02 |
| Decision Date | 1993-11-16 |