Last synced on 16 February 2024 at 11:04 pm

NOISE FILTER FOR PARADIGM MAGNETIC RESONANCE IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935570
510(k) Type
Traditional
Applicant
RESONEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1994
Days to Decision
118 days
Submission Type
Statement