Last synced on 23 February 2024 at 11:04 pm

MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934538
510(k) Type
Traditional
Applicant
NOISE CANCELLATION TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1994
Days to Decision
217 days
Submission Type
Summary