# K853586: Pressure Sensing Syringe 65000

- Pathway: 510(k) (Traditional)
- Applicant: Dlp, Inc.
- Decided: Nov 14, 1985 after 80 days
- Product code: DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 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
- K082725: Graftguard Pressure Controlling Syringe (2008), 5 descendants of its own
- K091733: Vasoview 6 Pro Endoscopic Vessel Harvesting System, Model VH-2500 (2009), 2 descendants of its own
- K191947: VASOVIEW HEMOPRO Extension Cable, VASOVIEW HEMOPRO 2 Extension Cable, Bipolar Extension Cable, Fixed Distance, Active Return Cord (2019), 0 descendants of its own
- K140603: Onepass Endoscopic Vessel Harvesting Sysyetm (2014), 0 descendants of its own
- K131659: Moerae Vein Preparation Kit (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K853586
Methodology: https://510kreport.com/methodology