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VIZTEK DR, MODELS: DR1000, DR3000, DR4000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082604
510(k) Type
Traditional
Applicant
Viztek, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2008
Days to Decision
74 days
Submission Type
Summary

VIZTEK DR, MODELS: DR1000, DR3000, DR4000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082604
510(k) Type
Traditional
Applicant
Viztek, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2008
Days to Decision
74 days
Submission Type
Summary