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CARDIAC MARKER CONTROL MODULE, MODEL CCCM

Page Type
Cleared 510(K)
510(k) Number
K983971
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1998
Days to Decision
9 days
Submission Type
Summary

CARDIAC MARKER CONTROL MODULE, MODEL CCCM

Page Type
Cleared 510(K)
510(k) Number
K983971
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1998
Days to Decision
9 days
Submission Type
Summary