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DUET SYSTEM

Page Type
Cleared 510(K)
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)
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