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HOLOGIC QDR X-RAY BONE DENSITOMETER, MODELS 1000, 2000, 4500, DELPHI, DISCOVERY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023398
510(k) Type
Special
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2002
Days to Decision
30 days
Submission Type
Summary

HOLOGIC QDR X-RAY BONE DENSITOMETER, MODELS 1000, 2000, 4500, DELPHI, DISCOVERY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023398
510(k) Type
Special
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2002
Days to Decision
30 days
Submission Type
Summary