# K200154: B&J DVT Compression Devices MHH800/MHH800SQ

- Pathway: 510(k) (Traditional)
- Applicant: B&J Manufacturing, Ltd.
- Decided: Jul 8, 2020 after 168 days
- Product code: JOW (Sleeve, Limb, Compressible)
- Device class: 2
- Regulation: 21 CFR 870.5800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K953648 (1996). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141064: Vesoflow Plus DVT Compression Device, Caremed Supply, Inc. (2014) Summary page 4.

## Most influential descendants
- K231801: MedHealth DVT compression Devices MHH900S/MHH900E (2023), 0 descendants of its own

## Indications for use
The B&J Manufacturing Ltd. MHH800 and MHH800SQ Deep Vein Thrombosis (DVT) Compression Devices are intended to increase venous blood flow in at risk patients in order to help prevent deep vein thrombosis.

Source page: https://510kreport.com/device/K200154
Methodology: https://510kreport.com/methodology