The following data is part of a premarket notification filed by Codan Us Corp. with the FDA for Iv Administration And Connect Sets.
| Device ID | K033301 |
| 510k Number | K033301 |
| Device Name: | IV ADMINISTRATION AND CONNECT SETS |
| Classification | Set, Administration, Intravascular |
| Applicant | CODAN US CORP. 3511 WEST SUNFLOWER AVE. Santa Ana, CA 92704 -6944 |
| Contact | Rohit Patel |
| Correspondent | Rohit Patel CODAN US CORP. 3511 WEST SUNFLOWER AVE. Santa Ana, CA 92704 -6944 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-10-14 |
| Decision Date | 2004-03-04 |