Medical Device Manufacturer · US , Canston , RI

Davol Inc., Sub. C. R. Bard, Inc. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1994

Recent clearances: VENTRALIGHT ST MESH, BARD PERFIX LIGHT PLUG, MODELS 0117050, 0117060, 0117070, 0117080, 0117150, 0117160, BARD 3DMAX MESH

24
Total
24
Cleared
0
Denied

Davol Inc., Sub. C. R. Bard, Inc. has 24 FDA 510(k) cleared medical devices. Based in Canston, US.

Historical record: 24 cleared submissions from 1994 to 2010. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Davol Inc., Sub. C. R. Bard, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Citech as regulatory consultant.

FDA 510(k) Regulatory Record - Davol Inc., Sub. C. R. Bard, Inc.

24 devices
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