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DUET SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061602
510(k) Type
Traditional
Applicant
BIOVIEW LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/23/2007
Days to Decision
229 days
Submission Type
Summary

DUET SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061602
510(k) Type
Traditional
Applicant
BIOVIEW LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/23/2007
Days to Decision
229 days
Submission Type
Summary