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MODEL 20 DIGITAL PULSE RATE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K780937
510(k) Type
Traditional
Applicant
SENTRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1978
Days to Decision
84 days

MODEL 20 DIGITAL PULSE RATE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K780937
510(k) Type
Traditional
Applicant
SENTRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1978
Days to Decision
84 days