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ACTIVASCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072848
510(k) Type
Special
Applicant
BIORETEC LTD
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
11/2/2007
Days to Decision
29 days
Submission Type
Summary

ACTIVASCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072848
510(k) Type
Special
Applicant
BIORETEC LTD
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
11/2/2007
Days to Decision
29 days
Submission Type
Summary