# K092893: Tytan Automatic Aneroid Sphygmomanometer, Model A730 and Manual Digital LCD Sphygmomanometer, Model A830 Series

- Pathway: 510(k) (Traditional)
- Applicant: Tytan Medical Corp.
- Decided: Jan 14, 2010 after 115 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K871718 (1987). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033025: Tytan Professional /Economy Series Sphygmomanometer, NO 710/NO 700, Tytan Medical Corp. (2003) Summary page 1.
- K061456: A & D Medical UM-101 Digital Blood Pressure Monitor, A&D Engineering, Inc. (2006) Summary page 1.

## Indications for use
The TYTAN Automatic Aneroid Sphygmomanometer model A730 and TYTAN Manual Digital LCD Sphygmomanometer model A830 are noninvasive blood pressure measurement systems intended to measure the systolic and diastolic blood pressures, at hospital or professional environment by using a non-invasive technique in which an inflatable cuff is wrapped around the upper arm.

Source page: https://510kreport.com/device/K092893
Methodology: https://510kreport.com/methodology