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MODIFICATION TO SUPEROPEN 0.23T MRI SYSTEM, MODEL NAM-P023A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082485
510(k) Type
Traditional
Applicant
NEUSOFT MEDICAL SYSTEMS CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/9/2008
Days to Decision
12 days
Submission Type
Summary