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HDR VISION, VISION HDR, HD R/F, UROMAT HD R/F

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081073
510(k) Type
Traditional
Applicant
Pausch, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2008
Days to Decision
234 days
Submission Type
Summary

HDR VISION, VISION HDR, HD R/F, UROMAT HD R/F

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081073
510(k) Type
Traditional
Applicant
Pausch, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2008
Days to Decision
234 days
Submission Type
Summary