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DTX-200 BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964562
510(k) Type
Traditional
Applicant
OSTEOMETER MEDITECH A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/1997
Days to Decision
282 days
Submission Type
Summary

DTX-200 BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964562
510(k) Type
Traditional
Applicant
OSTEOMETER MEDITECH A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/1997
Days to Decision
282 days
Submission Type
Summary