Embol-X, Inc.
Embol-X, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2003.
Top product codes for Embol-X, Inc.
Recent clearances by Embol-X, Inc.
- K022071 — EMBOL-X AORTIC FILTERS,ETRA-SMALL,SMALL,MEDIUM,LARGE,EXTRA LARGE,MODELS CF26000.CF29000,CF32000,CF35000,CF4000
- K020693 — AORTIC CANNULA, METAL J-TIP (24FR) MODEL #CF00100; AORTIC CANNULA, PLASTIC J-TIP (24FR) MODEL #CF00101
- K002973 — EMBOL-X INTRODUCER, MODEL CF00200
- K980631 — EMBOL-X AORTIC OCCLUSION AND CARDIOPLEGIA CANNULA
Data sourced from openFDA. This site is unofficial and independent of the FDA.