Medical Device Manufacturer · DK , Copenhagen

Multicept, Aps. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1985
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Multicept, Aps. Obstetrics & Gynecology

1 devices
1-1 of 1
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