# K191209: Aneroid Type Blood Pressure Kit

- Pathway: 510(k) (Traditional)
- Applicant: Dongguan Mars Medical Products Co., Ltd.
- Decided: Jun 18, 2019 after 43 days
- Product code: DXQ (Blood Pressure Cuff)
- Device class: 2
- Regulation: 21 CFR 870.1120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K780715 (1978). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K780715: Aneroid Type Blood Pressure Kit, Mars Metal Co., Ltd. (1978) Summary page 4.

## Indications for use
The device is intended to be used by medical professionals or in the home for the measurement of systolic and diastolic pressure. The models MS-200, MS-200D and MS-200M are intended to be manually attached to a patient and manually inflated along with a manual method.

Source page: https://510kreport.com/device/K191209
Methodology: https://510kreport.com/methodology