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CARDIAC FUNCTION LABORATORY; PRESSURE INTERFACE; PRESSURE / VOLUME CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003020
510(k) Type
Traditional
Applicant
CD LEYCOM BV
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/11/2001
Days to Decision
226 days
Submission Type
Summary

CARDIAC FUNCTION LABORATORY; PRESSURE INTERFACE; PRESSURE / VOLUME CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003020
510(k) Type
Traditional
Applicant
CD LEYCOM BV
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/11/2001
Days to Decision
226 days
Submission Type
Summary