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AUTOTUNE DEVICE (ATD II)/PHILIPS S-15/ACS MRI SCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932403
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1994
Days to Decision
297 days
Submission Type
Summary