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HEART SENTINEL

Page Type
Cleared 510(K)
510(k) Number
K802900
510(k) Type
Traditional
Applicant
TOTEMITE MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1981
Days to Decision
114 days

HEART SENTINEL

Page Type
Cleared 510(K)
510(k) Number
K802900
510(k) Type
Traditional
Applicant
TOTEMITE MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1981
Days to Decision
114 days