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CARDIOSTRESS

Page Type
Cleared 510(K)
510(k) Number
K820011
510(k) Type
Traditional
Applicant
INSTRUMENTS FOR CARDIAC RESEARCH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
17 days

CARDIOSTRESS

Page Type
Cleared 510(K)
510(k) Number
K820011
510(k) Type
Traditional
Applicant
INSTRUMENTS FOR CARDIAC RESEARCH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
17 days