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ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234033
510(k) Type
Traditional
Applicant
Boehringer Laboratories LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2024
Days to Decision
138 days
Submission Type
Summary

ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234033
510(k) Type
Traditional
Applicant
Boehringer Laboratories LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2024
Days to Decision
138 days
Submission Type
Summary