Medical Device Manufacturer · DK , Herlev

Osteometer Biotech A/S

2 submissions · 2 cleared · Since 1999
2
Total
2
Cleared
0
Denied

Osteometer Biotech A/S — FDA 510(k) Submissions

Osteometer Biotech A/S has submitted 2 FDA 510(k) premarket notifications since 1999, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Test, Osteocalcin, Column Chromatography & Color Development, Hydroxyproline . Use the specialty filter in the sidebar to narrow results.

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