# K832907: Invasive Monitoring Kits

- Pathway: 510(k) (Traditional)
- Applicant: American Pharmaseal Div. Ahsc
- Decided: Jan 10, 1984 after 134 days
- Product code: DRS (Transducer, Blood-Pressure, Extravascular)
- Device class: 2
- Regulation: 21 CFR 870.2850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K070384: Argon Continuous Flush Device (2007), 0 descendants of its own
- K062342: Truepulse Disposable Invasive Blood Pressure Monitoring Kit (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K832907
Methodology: https://510kreport.com/methodology