The following data is part of a premarket notification filed by Med Fusion Systems, Inc. with the FDA for Three Way Infusion Set.
| Device ID | K841882 |
| 510k Number | K841882 |
| Device Name: | THREE WAY INFUSION SET |
| Classification | Set, Administration, Intravascular |
| Applicant | MED FUSION SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-05-07 |
| Decision Date | 1984-06-05 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50351688509077 | K841882 | 000 |
| 50351688500319 | K841882 | 000 |
| 50351688510325 | K841882 | 000 |
| 50351688510448 | K841882 | 000 |
| 50351688510455 | K841882 | 000 |
| 50351688510462 | K841882 | 000 |
| 50351688510479 | K841882 | 000 |
| 50351688511599 | K841882 | 000 |
| 50351688511605 | K841882 | 000 |
| 50351688511971 | K841882 | 000 |
| 50351688511988 | K841882 | 000 |
| 50351688512008 | K841882 | 000 |
| 50351688512015 | K841882 | 000 |
| 50351688500784 | K841882 | 000 |
| 50351688508384 | K841882 | 000 |
| 50351688508445 | K841882 | 000 |
| 50351688500302 | K841882 | 000 |