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IntelliSpace Perinatal Rev.K.00

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173941
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/10/2018
Days to Decision
258 days
Submission Type
Summary

IntelliSpace Perinatal Rev.K.00

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173941
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/10/2018
Days to Decision
258 days
Submission Type
Summary