Last synced on 13 June 2025 at 11:06 pm

OPTION FOR THE QDR BONE DENSITOMETER, MODELS QDR4500, QDR2000, QDR1500, QDR4000, QDR1000, QDR1000W

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992775
510(k) Type
Traditional
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1999
Days to Decision
44 days
Submission Type
Summary

OPTION FOR THE QDR BONE DENSITOMETER, MODELS QDR4500, QDR2000, QDR1500, QDR4000, QDR1000, QDR1000W

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992775
510(k) Type
Traditional
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1999
Days to Decision
44 days
Submission Type
Summary