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FREEZOR XTRA SURGICAL CARDIAC CRYOABLATION DEVICE AND CCT.2 CARDIAC CARDIAC CRYOABLATION CRYOCONSOLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030303
510(k) Type
Traditional
Applicant
Cryocath Technologies, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/29/2003
Days to Decision
90 days
Submission Type
Summary

FREEZOR XTRA SURGICAL CARDIAC CRYOABLATION DEVICE AND CCT.2 CARDIAC CARDIAC CRYOABLATION CRYOCONSOLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030303
510(k) Type
Traditional
Applicant
Cryocath Technologies, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/29/2003
Days to Decision
90 days
Submission Type
Summary