Echocath, Inc.
Echocath, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2001.
Top product codes for Echocath, Inc.
Recent clearances by Echocath, Inc.
- K010482 — ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1
- K990642 — ECHOFLOW DOPPLER BLOOD VELOCITY METER
- K932436 — ECHOMARK INTRAUTERINE GUIDING CATHETER
- K933417 — ECHOMARK(R) ELECTROPHYSIOLOGY CATHETER
- K926351 — COLORMARK(TM) VISUALIZATION SYSTEM
- K922787 — ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION
Data sourced from openFDA. This site is unofficial and independent of the FDA.