The following data is part of a premarket notification filed by Cord Stick Corp. with the FDA for Cord Stick Multiple Draw System.
| Device ID | K031058 |
| 510k Number | K031058 |
| Device Name: | CORD STICK MULTIPLE DRAW SYSTEM |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | CORD STICK CORP. 1400 FLORIDA AVE., SUITE 205 Modesto, CA 95350 |
| Contact | Michael Moen |
| Correspondent | Michael Moen CORD STICK CORP. 1400 FLORIDA AVE., SUITE 205 Modesto, CA 95350 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-04-03 |
| Decision Date | 2003-06-13 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00861916000306 | K031058 | 000 |
| 0861916000304 | K031058 | 000 |
| 0861916000307 | K031058 | 000 |