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HOLOGIC QDR EXPLORER X-RAY BONE DENSITOMETER, MODEL EXPLORER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033224
510(k) Type
Special
Applicant
Hologic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
30 days
Submission Type
Summary

HOLOGIC QDR EXPLORER X-RAY BONE DENSITOMETER, MODEL EXPLORER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033224
510(k) Type
Special
Applicant
Hologic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2003
Days to Decision
30 days
Submission Type
Summary