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QWH-300 WRIST ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993819
510(k) Type
Special
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1999
Days to Decision
23 days
Submission Type
Statement

QWH-300 WRIST ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993819
510(k) Type
Special
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1999
Days to Decision
23 days
Submission Type
Statement