Last synced on 25 January 2026 at 3:41 am

CARDIOTHERM-500X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K771718
510(k) Type
Traditional
Applicant
COLUMBUS INSTRUMENTS INTL. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1977
Days to Decision
16 days

CARDIOTHERM-500X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K771718
510(k) Type
Traditional
Applicant
COLUMBUS INSTRUMENTS INTL. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1977
Days to Decision
16 days