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BLOOD PRESSURE MONITOR BP600X

Page Type
Cleared 510(K)
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)
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