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Arm Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192023
510(k) Type
Abbreviated
Applicant
Truly Instrument Limited
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/23/2019
Days to Decision
147 days
Submission Type
Summary

Arm Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192023
510(k) Type
Abbreviated
Applicant
Truly Instrument Limited
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/23/2019
Days to Decision
147 days
Submission Type
Summary