MNWClass II

Analyzer, Body Composition

21 CFR 870.2770 / Cardiovascular

MNW is the FDA product code for Analyzer, Body Composition, a class II device type, regulated under 21 CFR 870.2770. As of 2026-09-10, FDA records hold 79 510(k) clearances under this code, the most recent dated 2024-06-15, and no recalls.

Classification record

Product code: MNW
Device name: Analyzer, Body Composition
Regulation: 21 CFR 870.2770
Device class: Class II
Review panel: Cardiovascular
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 79
Ingested recalls: 0

Clearances, product code MNW

By decision year

79 clearances under product code MNW with a decision year between 1997 and 2024, 2011 the highest year at 11.

Show the numbers

510(k) clearances under FDA product code MNW by decision year
Year	Clearances
1997	2
1998	2
2000	1
2001	3
2002	1
2003	8
2004	4
2005	8
2006	8
2007	4
2008	4
2009	4
2010	1
2011	11
2012	4
2013	9
2014	3
2015	1
2024	1

Applicants with the most clearances

Product code MNW

Applicants holding the most 510(k) clearances under product code MNW
Applicant	Clearances
Biospace Inc.	9
Bodystat Ltd	7
Jawon Medical Co., Ltd.	5
Omron Healthcare Co., Ltd.	4
Tanita Corp. of America	4
Zhongshan Transtek Electronics Co., Ltd	4
Shenzhen Healthcare Electronic Technology Co., Ltd.	3
Aiia Communication, Inc.	2
Guangdong Transtek Medical Electronics Co.,Ltd	2
Impedimed, Inc.	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 34 companies shown, in name order