Medical Device Manufacturer · DK , Hoersholm

Multicept A/S - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Multicept A/S Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Mar 05, 2001

MULTI CARE THERAPEUTIC VIBRATOR

Obstetrics & Gynecology · 53d