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Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System

Page Type
Cleared 510(K)
510(k) Number
K163316
510(k) Type
Traditional
Applicant
CAREFUSION 303, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2017
Days to Decision
211 days
Submission Type
Summary

Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System

Page Type
Cleared 510(K)
510(k) Number
K163316
510(k) Type
Traditional
Applicant
CAREFUSION 303, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2017
Days to Decision
211 days
Submission Type
Summary