Koven and Assoc., Inc.
Koven and Assoc., Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1993.
Top product codes for Koven and Assoc., Inc.
Recent clearances by Koven and Assoc., Inc.
- K922669 — MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW
- K920333 — SMARTDOP 20 BI-DIRECTIONAL BLOOD FLOW DETECTOR
- K915550 — MINI DOPPLER II ULTRASOUND BLOOD FLOW DETECTOR
- K913595 — DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM
- K912409 — MODEL HD-207 BIDIRECTIONAL VELOCITY METER
- K903026 — ES-1000SP II SMART DOP
- K894892 — HD-2200 PNEUMO-DOP VASCULAR TESTING SYSTEM
- K892707 — DVM-4200 BLOOD FLOWMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.