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MODIFICATION TO DUET SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050840
510(k) Type
Traditional
Applicant
BIOVIEW LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/16/2005
Days to Decision
137 days
Submission Type
Summary

MODIFICATION TO DUET SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050840
510(k) Type
Traditional
Applicant
BIOVIEW LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/16/2005
Days to Decision
137 days
Submission Type
Summary