FDA 510(k) Applications Submitted by OSTEOMETER MEDITECH A/S
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K963789 | 09/20/1996 | DTX-100 BONE DENSITOMETER | OSTEOMETER MEDITECH A/S |
| K964562 | 11/13/1996 | DTX-200 BONE DENSITOMETER | OSTEOMETER MEDITECH A/S |
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