Last synced on 14 November 2025 at 11:06 pm

QUIK-CAP

Page Type
Cleared 510(K)
510(k) Number
K000865
510(k) Type
Traditional
Applicant
NEUROSCAN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2000
Days to Decision
32 days
Submission Type
Summary

QUIK-CAP

Page Type
Cleared 510(K)
510(k) Number
K000865
510(k) Type
Traditional
Applicant
NEUROSCAN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2000
Days to Decision
32 days
Submission Type
Summary