Last synced on 14 November 2025 at 11:06 pm

HRH-127-ALLEGRA HEAD ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K013508
510(k) Type
Special
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
29 days
Submission Type
Statement

HRH-127-ALLEGRA HEAD ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K013508
510(k) Type
Special
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
29 days
Submission Type
Statement