Angiometrx, Inc. is one of 24544 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Angiometrx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: METRICATH GEMINI-P BALLOON CATHETER, MODELS RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, METRICATH CONSOLE, MODEL 1000, METRICATH SYSTEM, METRICATH SYSTEM COMPRISED OF METRICATH 1000 CONSOLE & METRICATH BALLOON CATHETER
3
Total
3
Cleared
0
Denied
Angiometrx, Inc. has 3 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 3 cleared submissions from 2003 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Angiometrx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Angiometrx, Inc.
3 devices