Last synced on 1 March 2024 at 11:05 pm

MAGNETIZATION TRANSFER CONTRAST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922677
510(k) Type
Traditional
Applicant
RESONEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1992
Days to Decision
92 days
Submission Type
Statement