Angiometrx, Inc.

Angiometrx, Inc. holds 3 FDA 510(k) medical device clearances, first cleared 2003, most recent 2005.

Top product codes for Angiometrx, Inc.

DQO — Cardiovascular2 devices
LIT — Cardiovascular1 device

Recent clearances by Angiometrx, Inc.

K051042 — METRICATH GEMINI-P BALLOON CATHETER, MODELS RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, METRICATH CONSOLE, MODEL 1000Code LIT·2005-08-05
K042685 — METRICATH SYSTEMCode DQO·2004-11-18
K024000 — METRICATH SYSTEM COMPRISED OF METRICATH 1000 CONSOLE & METRICATH BALLOON CATHETERCode DQO·2003-06-26

Data sourced from openFDA. This site is unofficial and independent of the FDA.