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TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII

Page Type
Cleared 510(K)
510(k) Number
K011058
510(k) Type
Traditional
Applicant
MERIDIAN MEDICAL TECHNOLOGIES LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/23/2001
Days to Decision
200 days
Submission Type
Summary

TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII

Page Type
Cleared 510(K)
510(k) Number
K011058
510(k) Type
Traditional
Applicant
MERIDIAN MEDICAL TECHNOLOGIES LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/23/2001
Days to Decision
200 days
Submission Type
Summary