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COAG-I ANALYZER, ALPHA MODEL

Page Type
Cleared 510(K)
510(k) Number
K882444
510(k) Type
Traditional
Applicant
CARDIOVASCULAR DIAGNOSTIC SERVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1988
Days to Decision
72 days

COAG-I ANALYZER, ALPHA MODEL

Page Type
Cleared 510(K)
510(k) Number
K882444
510(k) Type
Traditional
Applicant
CARDIOVASCULAR DIAGNOSTIC SERVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1988
Days to Decision
72 days