FDA 510(k) Applications Submitted by ANGIOMETRX INC.

FDA 510(k) Number Submission Date Device Name Applicant
K024000 12/04/2002 METRICATH SYSTEM COMPRISED OF METRICATH 1000 CONSOLE & METRICATH BALLOON CATHETER ANGIOMETRX INC.
K051042 04/25/2005 METRICATH GEMINI-P BALLOON CATHETER, MODELS RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, METRICATH CONSOLE, MODEL 1000 ANGIOMETRX INC.
K042685 09/29/2004 METRICATH SYSTEM ANGIOMETRX INC.


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