# K213010: FEELject LDV (Low dead volume) syringe

- Pathway: 510(k) (Traditional)
- Applicant: Feeltech Co., Ltd.
- Decided: May 31, 2023 after 618 days
- Product code: QNQ (Low Dead Space Piston Syringe)
- Device class: 2
- Regulation: 21 CFR 880.5860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K771205 (1977). 22 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192551: 1ml Luer Slip or Luer Lock Syringe, Syringe with permanently attached needle, Safety Syringe with permanently attached needle, Jiangsu Caina Medical Co.,Ltd (2020) Summary page 4.

## Most influential descendants
- K231856: TopFine® LDS (Low Dead Space) Syringe (2 models (TS-LDS2334, TS-LDS2534)) (2024), 1 descendant of its own
- K252814: Profoject™ Low Dead Space Syringe /Profoject™ Tuberculin Syringe; Profoject™ Low Dead Space Syringe with Needle /Profoject™ Tuberculin Syringe with Needle; Profoject™ Low Dead Space Syringe with Permanent Needle /Profoject™ Tuberculin Syringe with Permanent Needle;  Profoject™ Low Dead Space Safety Syringe /Profoject™ Tuberculin Safety Syringe (2026), 0 descendants of its own

## Indications for use
FEELject LDV(Low dead volume) Syringe is intended for use to inject fluid into or withdraw fluids from the parts of body below the surface of the skin.

Source page: https://510kreport.com/device/K213010
Methodology: https://510kreport.com/methodology