The following data is part of a premarket notification filed by Corpak, Inc. with the FDA for Corflo 300 Pump.
| Device ID | K944750 |
| 510k Number | K944750 |
| Device Name: | CORFLO 300 PUMP |
| Classification | Pump, Infusion |
| Applicant | CORPAK, INC. 100 CHADDICK DR. Wheeling, IL 60090 |
| Contact | George Nassif |
| Correspondent | George Nassif CORPAK, INC. 100 CHADDICK DR. Wheeling, IL 60090 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Se Subject To Traking & Pms (PT) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-09-26 |
| Decision Date | 1995-06-19 |