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HRH-63 HEAD ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K002774
510(k) Type
Traditional
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2000
Days to Decision
71 days
Submission Type
Statement

HRH-63 HEAD ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K002774
510(k) Type
Traditional
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2000
Days to Decision
71 days
Submission Type
Statement