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BLOOD PRESSURE MONITOR BP600X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834441
510(k) Type
Traditional
Applicant
LIFELINE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1984
Days to Decision
157 days

BLOOD PRESSURE MONITOR BP600X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834441
510(k) Type
Traditional
Applicant
LIFELINE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1984
Days to Decision
157 days