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TONOTEST BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K800904
510(k) Type
Traditional
Applicant
RETLIF, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
44 days

TONOTEST BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K800904
510(k) Type
Traditional
Applicant
RETLIF, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
44 days