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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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