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ALLURA XPER FD OR TABLE SERIES; ALLURA XPER FD10 SERIES; ALLURA XPER FD20 SERIES; ALLURA XPER FD BIPLANE SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130842
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/21/2013
Days to Decision
55 days
Submission Type
Summary

ALLURA XPER FD OR TABLE SERIES; ALLURA XPER FD10 SERIES; ALLURA XPER FD20 SERIES; ALLURA XPER FD BIPLANE SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130842
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/21/2013
Days to Decision
55 days
Submission Type
Summary