Maquet, Inc.
Maquet, Inc. holds FDA 510(k) medical device clearance, cleared in 2004, with 2 FDA device recalls on record.
Top product codes for Maquet, Inc.
FDA recalls by Maquet, Inc.
- Z-0627-2013 — Maquet Yuno Extension Table Device Maquet GmbH & Co. KG Kehler Strabe 31 Baden-Wuerttemberg 76437 Rastatt,Germany Used to support the lower extremities immediately before during and after surgery. The extension device is mounted to the YUNO operating table. The product may only be operated by medically trained staff within the OR environment.
- Z-2210-2012 — Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222 932-1888 info.cp@maquet.com www.maquet.com Used to introduce blood and sterile solution to the circulation system during extracorporeal circulation procedures
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Maquet, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.