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XPress BCD Breast Compression Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163388
510(k) Type
Traditional
Applicant
XPress BCD, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2017
Days to Decision
229 days
Submission Type
Summary

XPress BCD Breast Compression Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163388
510(k) Type
Traditional
Applicant
XPress BCD, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2017
Days to Decision
229 days
Submission Type
Summary