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FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETER

Page Type
Cleared 510(K)
510(k) Number
K983269
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 EXPERT-XL BONE DENSITOMETER

Page Type
Cleared 510(K)
510(k) Number
K983269
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