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QDR-1000 AND QDR-1000/W 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
K905753
510(k) Type
Traditional
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1991
Days to Decision
168 days

QDR-1000 AND QDR-1000/W 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
K905753
510(k) Type
Traditional
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1991
Days to Decision
168 days