Cordis Corp., A Johnson & Johnson Co.

5FDA 510(k) medical device clearances.

Top product codes for Cordis Corp., A Johnson & Johnson Co.

Recent clearances by Cordis Corp., A Johnson & Johnson Co.

K140438 — MICRO GUIDE CATHETER ELITECode PDU·2014-11-14
K131225 — ADROIT GUIDING CATHETERCode DQY·2013-05-29
K091077 — OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETERCode DTK·2010-02-04
K083814 — OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120Code PDU·2009-01-13
K062531 — ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRECode NTE·2006-09-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.