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VIZION ULTRA

Page Type
Cleared 510(K)
510(k) Number
K133139
510(k) Type
Special
Applicant
VIZTEK LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2014
Days to Decision
168 days
Submission Type
Summary

VIZION ULTRA

Page Type
Cleared 510(K)
510(k) Number
K133139
510(k) Type
Special
Applicant
VIZTEK LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2014
Days to Decision
168 days
Submission Type
Summary