The following data is part of a premarket notification filed by Numed, Inc. with the FDA for Numed Z-5 Atrioseptostomy Catheter.
| Device ID | K001804 |
| 510k Number | K001804 |
| Device Name: | NUMED Z-5 ATRIOSEPTOSTOMY CATHETER |
| Classification | Catheter, Septostomy |
| Applicant | NUMED, INC. 2880 MAIN ST. Hopkinton, NY 12965 |
| Contact | Nichelle Laflesh |
| Correspondent | Nichelle Laflesh NUMED, INC. 2880 MAIN ST. Hopkinton, NY 12965 |
| Product Code | DXF |
| CFR Regulation Number | 870.5175 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-06-15 |
| Decision Date | 2000-07-12 |