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Spaulding Electrocardiograph 2100iQ

Page Type
Cleared 510(K)
510(k) Number
K150564
510(k) Type
Traditional
Applicant
Spaulding Clinical Research, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2015
Days to Decision
159 days
Submission Type
Summary

Spaulding Electrocardiograph 2100iQ

Page Type
Cleared 510(K)
510(k) Number
K150564
510(k) Type
Traditional
Applicant
Spaulding Clinical Research, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2015
Days to Decision
159 days
Submission Type
Summary