The following data is part of a premarket notification filed by Electromed Intl., Ltd. with the FDA for Cardio-respiratory Monitor Model Cr-1.
| Device ID | K821959 |
| 510k Number | K821959 |
| Device Name: | CARDIO-RESPIRATORY MONITOR MODEL CR-1 |
| Classification | Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) |
| Applicant | ELECTROMED INTL., LTD. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DRT |
| CFR Regulation Number | 870.2300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-06-30 |
| Decision Date | 1982-07-20 |