JOMClass II

Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

21 CFR 870.2780 / Cardiovascular

JOM is the FDA product code for Plethysmograph, Photoelectric, Pneumatic Or Hydraulic, a class II device type, regulated under 21 CFR 870.2780. As of 2026-09-10, FDA records hold 53 510(k) clearances under this code, the most recent dated 2022-10-20, and no recalls.

Classification record

Product code: JOM
Device name: Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Regulation: 21 CFR 870.2780
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: Yes
Ingested clearances: 53
Ingested recalls: 0

Clearances, product code JOM

By decision year

53 clearances under product code JOM with a decision year between 1976 and 2022, 1979 the highest year at 4.

Show the numbers

510(k) clearances under FDA product code JOM by decision year
Year	Clearances
1976	1
1977	1
1978	1
1979	4
1980	1
1981	1
1983	3
1985	3
1986	1
1987	3
1988	3
1989	2
1990	1
1991	1
1995	1
1997	1
1998	1
1999	2
2002	1
2003	2
2004	1
2007	2
2009	1
2010	2
2011	1
2012	1
2013	2
2015	2
2017	1
2018	1
2020	2
2021	1
2022	2

Applicants with the most clearances

Product code JOM

Applicants holding the most 510(k) clearances under product code JOM
Applicant	Clearances
D. E. Hokanson, Inc.	5
Biomedix Wai	3
LD Technology LLC	2
Life Sciences Manufacturing, Inc.	2
Medasonics, Inc.	2
Medicore Co. Ltd.	2
Mesi d.o.o.; Mesi, Development of Medical Devices, Ltd.	2
Sonicaid, Inc.	2
Vasocor, Inc.	2
Advanced Medical Technology, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 23 companies shown, in name order