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NEOCOIL 1.5T 16 CHANNEL CARDIAC-ABDOMINAL-PELVIC ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073181
510(k) Type
Traditional
Applicant
NEOCOIL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2007
Days to Decision
8 days
Submission Type
Summary

NEOCOIL 1.5T 16 CHANNEL CARDIAC-ABDOMINAL-PELVIC ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073181
510(k) Type
Traditional
Applicant
NEOCOIL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2007
Days to Decision
8 days
Submission Type
Summary