Last synced on 25 January 2026 at 3:41 am

BIOPSY DIGIT-AM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062039
510(k) Type
Traditional
Applicant
Giotto USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2006
Days to Decision
54 days
Submission Type
Summary

BIOPSY DIGIT-AM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062039
510(k) Type
Traditional
Applicant
Giotto USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2006
Days to Decision
54 days
Submission Type
Summary