C. R. Bard
C. R. Bard holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2020.
Top product codes for C. R. Bard
Recent clearances by C. R. Bard
- K190527 — GlidePath Long-Term Hemodialysis Catheters, HemoStar Long-Term Hemodialysis Catheters, HemoStar XK Long-Term Hemodialysis Catheters
- K182281 — Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech
- K172571 — ULTRASCORE Focused Force PTA Balloon
- K170294 — VENTRALIGHT ST Mesh with ECHO 2 Positioning System 11cm (4.5) Circle, VENTRALIGHT ST Mesh with ECHO 2 Positioning System 10cm x 15cm (4x 6) Ellipse, VENTRALIGHT ST Mesh with ECHO 2 Positioning System 15cm (6) Circle, VENTRALIGHT ST Mesh with ECHO 2 Positioning System 15cm x 20cm (6x8) Ellipse, VENTRALIGHT ST Mesh with ECHO 2 Positioning System 15cm x 25cm (6x10) Oval
- K162193 — XenMatrix AB Surgical Graft
- K151177 — XenMatrix AB Surgical Graft
- K142818 — Phasix Mesh
- K140501 — XENMATRIX SURGICAL GRAFT
- K112791 — SITESCRUB IPA DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.