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

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