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PARAGON 420, CARDIAC MONITOR

Page Type
Cleared 510(K)
510(k) Number
K861067
510(k) Type
Traditional
Applicant
LIFE SENSING INSTRUMENT COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1986
Days to Decision
77 days

PARAGON 420, CARDIAC MONITOR

Page Type
Cleared 510(K)
510(k) Number
K861067
510(k) Type
Traditional
Applicant
LIFE SENSING INSTRUMENT COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1986
Days to Decision
77 days