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NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070778
510(k) Type
Traditional
Applicant
NEOCOIL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2007
Days to Decision
21 days
Submission Type
Summary

NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070778
510(k) Type
Traditional
Applicant
NEOCOIL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2007
Days to Decision
21 days
Submission Type
Summary