Last synced on 14 November 2025 at 11:06 pm

CARDIOCAP II(TM)

Page Type
Cleared 510(K)
510(k) Number
K912530
510(k) Type
Traditional
Applicant
DATEX MEDICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1991
Days to Decision
90 days
Submission Type
Statement

CARDIOCAP II(TM)

Page Type
Cleared 510(K)
510(k) Number
K912530
510(k) Type
Traditional
Applicant
DATEX MEDICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1991
Days to Decision
90 days
Submission Type
Statement