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PHILIPS GYROSCAN T5 SERIES II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920578
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1992
Days to Decision
270 days
Submission Type
Summary