# K221860: PLPT LDV (Low Dead Volume) LC (Luer-Cone) Sterile Syringe, PLPT LDV (Low Dead Volume) LL (Luer-Lock) Sterile Syringe

- Pathway: 510(k) (Traditional)
- Applicant: Poonglim Pharmatech, Inc.
- Decided: Sep 15, 2023 after 445 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: 9 generations back to K771205 (1977). 29 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K210443: PLPT LDV (Low Dead Volume) Sterile Syringe, Poonglim Pharmatech, Inc. (2021) Summary page 4.
- K210444: EZ-Injec LDV Sterile Safety Needle, Poonglim Pharmatech, Inc. (2021) Summary page 4.

## Most influential descendants
- K241190: PLPT LDV (Low Dead Volume) LC (Luer-Cone) Sterile Syringe; PLPT LDV (Low Dead Volume) LL (Luer-Lock) Sterile Syringe (2024), 0 descendants of its own

## Indications for use
PLPT LDV (Low Dead Volume) LC(Luer-Cone) Sterile Syringe / PLPT LDV (Low Dead Volume) LL(Luer-Lock) Sterile Syringe is intended for use by health care professionals for general purpose aspiration of fluid from vials, ampoules and liquid injection below the surface of the skin.

Source page: https://510kreport.com/device/K221860
Methodology: https://510kreport.com/methodology