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S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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