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NEUROQ 3.6

Page Type
Cleared 510(K)
510(k) Number
K130451
510(k) Type
Traditional
Applicant
SYNTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2013
Days to Decision
84 days
Submission Type
Summary

NEUROQ 3.6

Page Type
Cleared 510(K)
510(k) Number
K130451
510(k) Type
Traditional
Applicant
SYNTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2013
Days to Decision
84 days
Submission Type
Summary