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Philips IntelliVue XDS Software

Page Type
Cleared 510(K)
510(k) Number
K182637
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/26/2019
Days to Decision
214 days
Submission Type
Summary

Philips IntelliVue XDS Software

Page Type
Cleared 510(K)
510(k) Number
K182637
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/26/2019
Days to Decision
214 days
Submission Type
Summary