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FB-100U SERIES DIGITAL BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K070209
510(k) Type
Traditional
Applicant
FEGO PRECISION INDUSTRIAL CO; LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2007
Days to Decision
198 days
Submission Type
Summary

FB-100U SERIES DIGITAL BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K070209
510(k) Type
Traditional
Applicant
FEGO PRECISION INDUSTRIAL CO; LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2007
Days to Decision
198 days
Submission Type
Summary