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DISCOVERY 3T 16 CH BODY ARRAY COIL (ANTERIOR); DISCOVERY 3T 16 CH BODY ARRAY COIL (POSTERIOR); DISCOVERY 3T 32 CH BODY A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103365
510(k) Type
Traditional
Applicant
GE HEALTHCARE COILS (USA INSTRUMENTS INC.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2011
Days to Decision
56 days
Submission Type
Summary

DISCOVERY 3T 16 CH BODY ARRAY COIL (ANTERIOR); DISCOVERY 3T 16 CH BODY ARRAY COIL (POSTERIOR); DISCOVERY 3T 32 CH BODY A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103365
510(k) Type
Traditional
Applicant
GE HEALTHCARE COILS (USA INSTRUMENTS INC.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2011
Days to Decision
56 days
Submission Type
Summary