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Philips CombiDiagnost R90

Page Type
Cleared 510(K)
510(k) Number
K163210
510(k) Type
Traditional
Applicant
Philips Medical Systems DMC GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/31/2017
Days to Decision
77 days
Submission Type
Summary

Philips CombiDiagnost R90

Page Type
Cleared 510(K)
510(k) Number
K163210
510(k) Type
Traditional
Applicant
Philips Medical Systems DMC GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/31/2017
Days to Decision
77 days
Submission Type
Summary