# K083686: Baixin Disposable Syringe, Multiple Sizes

- Pathway: 510(k) (Traditional)
- Applicant: Anhui Kangda Medical Products Co., Ltd.
- Decided: Jul 2, 2009 after 202 days
- Product code: FMF (Syringe, Piston)
- 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The intended use of the BAIXIN Disposable Syringe is to inject fluids into or withdraw fluids from the body.

Source page: https://510kreport.com/device/K083686
Methodology: https://510kreport.com/methodology