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PHILIPS ENDO-CAVITARY MRI COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
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510(k) Number
K930193
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS, INC.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
6/24/1994
Days to Decision
526 days
Submission Type
Summary