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DPX BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873296
510(k) Type
Traditional
Applicant
LUNAR RADIATION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/1988
Days to Decision
294 days

DPX BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873296
510(k) Type
Traditional
Applicant
LUNAR RADIATION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/1988
Days to Decision
294 days