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HTS 820 CARDIAC MONITOR

Page Type
Cleared 510(K)
510(k) Number
K896967
510(k) Type
Traditional
Applicant
LIFE SENSING INSTRUMENT COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1990
Days to Decision
91 days

HTS 820 CARDIAC MONITOR

Page Type
Cleared 510(K)
510(k) Number
K896967
510(k) Type
Traditional
Applicant
LIFE SENSING INSTRUMENT COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1990
Days to Decision
91 days