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FRACTURE RISK ASSESSMENT OPTION FOR DPX SERIES BONE DENSITOMETERS

Page Type
Cleared 510(K)
510(k) Number
K983271
510(k) Type
Traditional
Applicant
LUNAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1998
Days to Decision
62 days
Submission Type
Summary

FRACTURE RISK ASSESSMENT OPTION FOR DPX SERIES BONE DENSITOMETERS

Page Type
Cleared 510(K)
510(k) Number
K983271
510(k) Type
Traditional
Applicant
LUNAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1998
Days to Decision
62 days
Submission Type
Summary