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MICROLIFE AUTOMATIC BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K970211
510(k) Type
Traditional
Applicant
MICRO WEISS ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1998
Days to Decision
464 days
Submission Type
Summary

MICROLIFE AUTOMATIC BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K970211
510(k) Type
Traditional
Applicant
MICRO WEISS ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1998
Days to Decision
464 days
Submission Type
Summary