Echocath, Inc.
Echocath, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Mar 20, 2001.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K010482 | ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1 | Mar 20, 2001 |
| K990642 | ECHOFLOW DOPPLER BLOOD VELOCITY METER | Sep 16, 1999 |
| K932436 | ECHOMARK INTRAUTERINE GUIDING CATHETER | Nov 16, 1995 |
| K933417 | ECHOMARK(R) ELECTROPHYSIOLOGY CATHETER | May 4, 1995 |
| K926351 | COLORMARK(TM) VISUALIZATION SYSTEM | Sep 16, 1993 |
| K922787 | ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION | Jan 6, 1993 |