The following data is part of a premarket notification filed by Clinical Data, Inc. with the FDA for Centurion Chart Recorder.
| Device ID | K822432 |
| 510k Number | K822432 |
| Device Name: | CENTURION CHART RECORDER |
| Classification | Recorder, Paper Chart |
| Applicant | CLINICAL DATA, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DSF |
| CFR Regulation Number | 870.2810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-08-12 |
| Decision Date | 1982-11-01 |