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MIDMARK DIAGNOSTICS IQMARK VITAL SIGNS MONITOR

Page Type
Cleared 510(K)
510(k) Number
K072516
510(k) Type
Traditional
Applicant
MIDMARK DIAGNOSTICS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2007
Days to Decision
41 days
Submission Type
Summary

MIDMARK DIAGNOSTICS IQMARK VITAL SIGNS MONITOR

Page Type
Cleared 510(K)
510(k) Number
K072516
510(k) Type
Traditional
Applicant
MIDMARK DIAGNOSTICS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2007
Days to Decision
41 days
Submission Type
Summary