Medical Device Manufacturer · DK , Dk-8721 Daugaard

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

2 submissions · 2 cleared · Since 2001
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Ronvig A/S Dental ✕

2 devices
1-2 of 2
Cleared Dec 22, 2003
B&R DEVICE
K032925 · EGS
Dental · 91d
Cleared May 10, 2001
DENTO-PREP PARTICLE MICROBLASTER
K010816 · KOJ
Dental · 52d
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