The following data is part of a premarket notification filed by Maquet Critical Care Ab with the FDA for Maquet Flow-i C20, Maquet Flow-i C30, Model 66 77 200, 66 77 30.
Device ID | K102182 |
510k Number | K102182 |
Device Name: | MAQUET FLOW-I C20, MAQUET FLOW-I C30, MODEL 66 77 200, 66 77 30 |
Classification | Gas-machine, Anesthesia |
Applicant | MAQUET CRITICAL CARE AB 45 BORBOUR POND DRIVE Wayne, NJ 07470 |
Contact | Whitney Torning |
Correspondent | Whitney Torning MAQUET CRITICAL CARE AB 45 BORBOUR POND DRIVE Wayne, NJ 07470 |
Product Code | BSZ |
CFR Regulation Number | 868.5160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-08-03 |
Decision Date | 2011-05-09 |
Summary: | summary |