Last synced on 23 May 2025 at 11:06 pm

PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022899
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2002
Days to Decision
80 days
Submission Type
Summary

PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022899
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2002
Days to Decision
80 days
Submission Type
Summary