Last synced on 18 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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