# K103715: Compass Vascular Access / Access Port / Lumbar Puncture / Intracranial Pressure

- Pathway: 510(k) (Special)
- Applicant: Mirador Biomedical, Inc.
- Decided: Jan 20, 2011 after 30 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.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K112203: Compass Global Pressure, Compass Thoracentesis, Paracentesis, Compartment Pressure, Epidural Assist, Arterial Assist (2011), 4 descendants of its own
- K142245: EpiAccess System (2014), 1 descendant of its own
- K133624: Compass CT, Compass CT Port (2014), 1 descendant of its own
- K170831: EpiAccess System (2017), 0 descendants of its own
- K161408: Compass Cast and MAP (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K103715
Methodology: https://510kreport.com/methodology