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CardioChek Plus Test System, CardioChek Home Test System, CardioChek PA Test System, CardioChek PA Home Test System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151545
510(k) Type
Traditional
Applicant
POLYMER TECHNOLOGY SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2016
Days to Decision
562 days
Submission Type
Summary

CardioChek Plus Test System, CardioChek Home Test System, CardioChek PA Test System, CardioChek PA Home Test System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151545
510(k) Type
Traditional
Applicant
POLYMER TECHNOLOGY SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2016
Days to Decision
562 days
Submission Type
Summary