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QUANTITATIVE NEUROQ 3.0

Page Type
Cleared 510(K)
510(k) Number
K072307
510(k) Type
Traditional
Applicant
SYNTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2008
Days to Decision
210 days
Submission Type
Summary

QUANTITATIVE NEUROQ 3.0

Page Type
Cleared 510(K)
510(k) Number
K072307
510(k) Type
Traditional
Applicant
SYNTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2008
Days to Decision
210 days
Submission Type
Summary