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AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050413
510(k) Type
Traditional
Applicant
Amplife Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2005
Days to Decision
14 days
Submission Type
Summary

AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050413
510(k) Type
Traditional
Applicant
Amplife Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2005
Days to Decision
14 days
Submission Type
Summary