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PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031333
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/13/2003
Days to Decision
15 days
Submission Type
Summary

PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031333
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/13/2003
Days to Decision
15 days
Submission Type
Summary