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Digital Automatic Blood Pressure Monitor BPM41 Series, Digital Automatic Blood Pressure Monitor BPM45 Series

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163648
510(k) Type
Traditional
Applicant
Grandway Technology (Shenzhen) Limited
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/7/2017
Days to Decision
196 days
Submission Type
Summary

Digital Automatic Blood Pressure Monitor BPM41 Series, Digital Automatic Blood Pressure Monitor BPM45 Series

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163648
510(k) Type
Traditional
Applicant
Grandway Technology (Shenzhen) Limited
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/7/2017
Days to Decision
196 days
Submission Type
Summary