510(k) K102182

MAQUET FLOW-I C20, MAQUET FLOW-I C30, MODEL 66 77 200, 66 77 30 by Maquet Critical Care AB — Product Code BSZ

K102182 is an FDA 510(k) premarket notification submitted by Maquet Critical Care AB for the device "MAQUET FLOW-I C20, MAQUET FLOW-I C30, MODEL 66 77 200, 66 77 30". The FDA issued a decision of Substantially Equivalent on May 9, 2011. The device falls under product code BSZ (Gas-Machine, Anesthesia), a Class II device regulated under 21 CFR 868.5160. Maquet Critical Care AB has at least 10 other 510(k) clearances on record.