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SYMPULSE COMPUTER SYSTEM FOR FONAR MRI SCANNERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003453
510(k) Type
Traditional
Applicant
FONAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2001
Days to Decision
72 days
Submission Type
Summary