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CATHETER, THERMAL DILUTION, OPEN CHEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760067
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1976
Days to Decision
35 days

CATHETER, THERMAL DILUTION, OPEN CHEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760067
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1976
Days to Decision
35 days