The following data is part of a premarket notification filed by Koven And Assoc., Inc. with the FDA for Ds-240 Ambulatory Blood Pressure Monitoring System.
| Device ID | K913595 |
| 510k Number | K913595 |
| Device Name: | DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | KOVEN AND ASSOC., INC. THE TRADE CENTER 300 BROOKES DRIVE, SUITE 105 St. Louis, MO 63042 |
| Contact | Paul G Koven |
| Correspondent | Paul G Koven KOVEN AND ASSOC., INC. THE TRADE CENTER 300 BROOKES DRIVE, SUITE 105 St. Louis, MO 63042 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-08-13 |
| Decision Date | 1992-03-27 |