The following data is part of a premarket notification filed by Douglas Scientific Products with the FDA for Bradycardia Alarm.
| Device ID | K813174 |
| 510k Number | K813174 |
| Device Name: | BRADYCARDIA ALARM |
| Classification | Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) |
| Applicant | DOUGLAS SCIENTIFIC PRODUCTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DRT |
| CFR Regulation Number | 870.2300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-06 |
| Decision Date | 1982-01-22 |