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MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY

Page Type
Cleared 510(K)
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

MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY

Page Type
Cleared 510(K)
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