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CLEARMRI HELIOS-RG8 COIL ACCESSORY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132381
510(k) Type
Traditional
Applicant
CLEARMRI SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2014
Days to Decision
247 days
Submission Type
Summary