Koven and Assoc., Inc.
Koven and Assoc., Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 29, 1993.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K922669 | MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW | January 29, 1993 |
| K920333 | SMARTDOP 20 BI-DIRECTIONAL BLOOD FLOW DETECTOR | January 22, 1993 |
| K915550 | MINI DOPPLER II ULTRASOUND BLOOD FLOW DETECTOR | December 10, 1992 |
| K913595 | DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM | March 27, 1992 |
| K912409 | MODEL HD-207 BIDIRECTIONAL VELOCITY METER | December 23, 1991 |
| K903026 | ES-1000SP II SMART DOP | February 26, 1991 |
| K894892 | HD-2200 PNEUMO-DOP VASCULAR TESTING SYSTEM | October 27, 1989 |
| K892707 | DVM-4200 BLOOD FLOWMETER | July 28, 1989 |