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CARDIOSPEX(TM) LIQUID CKMB/LD-1 IMMUNOINHIBITION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K946146
510(k) Type
Traditional
Applicant
CLINICAL CONTROLS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1995
Days to Decision
39 days
Submission Type
Statement

CARDIOSPEX(TM) LIQUID CKMB/LD-1 IMMUNOINHIBITION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K946146
510(k) Type
Traditional
Applicant
CLINICAL CONTROLS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1995
Days to Decision
39 days
Submission Type
Statement