# K071269: Hemodraw Arterial Blood Sampling System

- Pathway: 510(k) (Traditional)
- Applicant: Smiths Medical Asd, Inc.
- Decided: Aug 1, 2007 after 86 days
- Product code: CBT (Arterial Blood Sampling Kit)
- Device class: 1
- Regulation: 21 CFR 868.1100
- 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; 1 cites 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K163172: HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer Kit (2017), 2 descendants of its own
- K172458: HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer Kit (2017), 1 descendant of its own
- K221782: Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes (2023), 0 descendants of its own

## Indications for use
The HemoDrawTM Arterial Blood Sampling Set is a hemodynamic pressure monitoring and blood gas sampling system designed to allow easy withdrawal of blood samples from an arterial pressure monitoring line while maintaining a completely closed system.

Source page: https://510kreport.com/device/K071269
Methodology: https://510kreport.com/methodology