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HOLOGIC QDR X-RAY BONE DENSITOMETER/MODELS SERIES 4500, 4000, 2000, 1000 AND HOLOGIC DELPHI X-RAY BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002711
510(k) Type
Traditional
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2000
Days to Decision
28 days
Submission Type
Summary

HOLOGIC QDR X-RAY BONE DENSITOMETER/MODELS SERIES 4500, 4000, 2000, 1000 AND HOLOGIC DELPHI X-RAY BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002711
510(k) Type
Traditional
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2000
Days to Decision
28 days
Submission Type
Summary