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SkyPlate Detector for Philips Radiography/Fluoroscopy Systems

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171461
510(k) Type
Traditional
Applicant
Philips Medical Systems DMC GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/7/2017
Days to Decision
50 days
Submission Type
Summary

SkyPlate Detector for Philips Radiography/Fluoroscopy Systems

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171461
510(k) Type
Traditional
Applicant
Philips Medical Systems DMC GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/7/2017
Days to Decision
50 days
Submission Type
Summary