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DPX-RX BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982267
510(k) Type
Traditional
Applicant
Lunar Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1998
Days to Decision
50 days
Submission Type
Summary

DPX-RX BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982267
510(k) Type
Traditional
Applicant
Lunar Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1998
Days to Decision
50 days
Submission Type
Summary