Last synced on 16 May 2025 at 11:05 pm

PHILIPS XRG 90 X-RAY GENERATOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933650
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1993
Days to Decision
72 days
Submission Type
Summary

PHILIPS XRG 90 X-RAY GENERATOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933650
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1993
Days to Decision
72 days
Submission Type
Summary