The following data is part of a premarket notification filed by Waters Assoc., Inc. with the FDA for Cardiac Computers, Co-10 & Co-10r.
| Device ID | K781805 |
| 510k Number | K781805 |
| Device Name: | CARDIAC COMPUTERS, CO-10 & CO-10R |
| Classification | Computer, Diagnostic, Pre-programmed, Single-function |
| Applicant | WATERS ASSOC., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXG |
| CFR Regulation Number | 870.1435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-10-24 |
| Decision Date | 1979-01-29 |