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SINGLE BED ARRHYTHMIA MONITOR AM500

Page Type
Cleared 510(K)
510(k) Number
K831638
510(k) Type
Traditional
Applicant
LIFELINE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1983
Days to Decision
175 days

SINGLE BED ARRHYTHMIA MONITOR AM500

Page Type
Cleared 510(K)
510(k) Number
K831638
510(k) Type
Traditional
Applicant
LIFELINE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1983
Days to Decision
175 days