Sulzer Carbomedics, Inc.
Sulzer Carbomedics, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2002.
Top product codes for Sulzer Carbomedics, Inc.
Recent clearances by Sulzer Carbomedics, Inc.
- K023185 — ANNULOFLEX ANNUOPLASTY SYSTEM, MODEL AF 800
- K013022 — SULZER VASCUTEK GELWEAVE VALSALVA VASCULAR PROSTHESIS
- K021051 — ANNULOFLO SYSTEM, MITRAL MODEL AR700
- K002007 — SULZER VASCUTEK GELSOFT ERS VASCULAR PROSTHESIS
- K993288 — SULZER CARBOMEDICS CARDIOFIX PERICARDIUM
- K992056 — ANNULOFLEX ANNULOPLASTY SYSTEM, MODEL AF800
- K974648 — SULZER CARBOMEDICS LOW PROFILE MITRAL ROTATOR
- K972201 — PATCH,PLEDGET AND INTRACARDIAC,PETP,PTFE,POLYPROPYLENE
Data sourced from openFDA. This site is unofficial and independent of the FDA.