# K896514: QS90 Smooth E Arterial Blood Sampler

- Pathway: 510(k) (Traditional)
- Applicant: Radiometer America, Inc.
- Decided: Jan 23, 1990 after 70 days
- Product code: GIM (Tubes, Vacuum Sample, With Anticoagulant)
- Device class: 2
- Regulation: 21 CFR 862.1675
- 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; 2 cite 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
- K982922: Vacutainer Brand Blood Collection Syringe (1998), 3 descendants of its own
- K022426: BD Preset Blood Collection Syringe, BD a-Line Blood Collection Syringe, Models 365313, 365323,365316,365356,365373,36538 (2002), 2 descendants of its own
- K962158: Pico Models 30, 50, 70 (1996), 1 descendant of its own
- K260128: BD Preset™ and BD A-Line™ Arterial Blood Collection Syringes (2026), 0 descendants of its own
- K202446: BD Preset Syringe & BD A-Line Syringe (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K896514
Methodology: https://510kreport.com/methodology