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S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0

Page Type
Cleared 510(K)
510(k) Number
K002116
510(k) Type
Special
Applicant
MEDICAL DEVICE CONSULTANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2000
Days to Decision
27 days
Submission Type
Summary

S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0

Page Type
Cleared 510(K)
510(k) Number
K002116
510(k) Type
Special
Applicant
MEDICAL DEVICE CONSULTANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2000
Days to Decision
27 days
Submission Type
Summary