Last synced on 25 January 2026 at 3:41 am

METRICATH GEMINI-P BALLOON CATHETER, MODELS RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, METRICATH CONSOLE, MODEL 1000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051042
510(k) Type
Traditional
Applicant
Angiometrx, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
8/5/2005
Days to Decision
102 days
Submission Type
Summary

METRICATH GEMINI-P BALLOON CATHETER, MODELS RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, METRICATH CONSOLE, MODEL 1000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051042
510(k) Type
Traditional
Applicant
Angiometrx, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
8/5/2005
Days to Decision
102 days
Submission Type
Summary