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SENTINEL PULSE OXIMETER

Page Type
Cleared 510(K)
510(k) Number
K880672
510(k) Type
Traditional
Applicant
SENTINEL MONITORING TECHNOLOGIES, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1988
Days to Decision
77 days

SENTINEL PULSE OXIMETER

Page Type
Cleared 510(K)
510(k) Number
K880672
510(k) Type
Traditional
Applicant
SENTINEL MONITORING TECHNOLOGIES, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1988
Days to Decision
77 days