The following data is part of a premarket notification filed by Diasonics, Inc. with the FDA for Cardiovue Accessory Cart.
| Device ID | K820033 |
| 510k Number | K820033 |
| Device Name: | CARDIOVUE ACCESSORY CART |
| Classification | Recorder, Paper Chart |
| Applicant | DIASONICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DSF |
| CFR Regulation Number | 870.2810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-01-06 |
| Decision Date | 1982-01-22 |