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DIGITAL AUTOMATIC WRIST BLOOD PRESSURE MONITOR WBPM22 SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133618
510(k) Type
Traditional
Applicant
GRANDWAY TECHNOLOGY (SHENZHEN) LIMITED
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/5/2014
Days to Decision
100 days
Submission Type
Summary

DIGITAL AUTOMATIC WRIST BLOOD PRESSURE MONITOR WBPM22 SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133618
510(k) Type
Traditional
Applicant
GRANDWAY TECHNOLOGY (SHENZHEN) LIMITED
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/5/2014
Days to Decision
100 days
Submission Type
Summary