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RESTGRID PACKAGE/GYROSCAN NT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982834
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1998
Days to Decision
78 days
Submission Type
Summary