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TREX MRI MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K982157
510(k) Type
Traditional
Applicant
FIELD EFFECTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1998
Days to Decision
75 days
Submission Type
Summary

TREX MRI MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K982157
510(k) Type
Traditional
Applicant
FIELD EFFECTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1998
Days to Decision
75 days
Submission Type
Summary