# K962655: Aneroid and Mercurial Sphygmomanometers

- Pathway: 510(k) (Traditional)
- Applicant: American Diagnostic Corp.
- Decided: Jan 27, 1997 after 203 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
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K143332: Fast Sphyg by Koven (2015), 0 descendants of its own
- K071075: Terumo Digital Blood Pressure Monitor ES-H55A (2007), 0 descendants of its own
- K012553: Gsibp Blood Pressure Cuff (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K962655
Methodology: https://510kreport.com/methodology