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AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043550
510(k) Type
Traditional
Applicant
AMPLIFE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2005
Days to Decision
35 days
Submission Type
Summary

AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043550
510(k) Type
Traditional
Applicant
AMPLIFE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2005
Days to Decision
35 days
Submission Type
Summary