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PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K130056
510(k) Type
Traditional
Applicant
LD TECHNOLOGY LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2013
Days to Decision
92 days
Submission Type
Summary

PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K130056
510(k) Type
Traditional
Applicant
LD TECHNOLOGY LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2013
Days to Decision
92 days
Submission Type
Summary