The following data is part of a premarket notification filed by Promex, Inc. with the FDA for Co-axial Introducer Needle.
| Device ID | K022634 |
| 510k Number | K022634 |
| Device Name: | CO-AXIAL INTRODUCER NEEDLE |
| Classification | Introducer, Catheter |
| Applicant | PROMEX, INC. 3049 HUDSON ST. Franklin, IN 46131 |
| Contact | Joseph L Mark |
| Correspondent | Joseph L Mark PROMEX, INC. 3049 HUDSON ST. Franklin, IN 46131 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-08-08 |
| Decision Date | 2002-11-06 |