# K993609: Sologuard Locking Plus Syringe

- Pathway: 510(k) (Traditional)
- Applicant: Safeguard Medical Products, Inc.
- Decided: Mar 17, 2000 after 144 days
- Product code: MEG (Syringe, Antistick)
- 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 its predicate without a number.
- (no number) Becton Dickinson Single Use Hypodermic Syringes: named in the summary without a submission number

## Indications for use
These syringes are intended for use by health care professionals for general purpose fluid aspiration/injection. The devices contain a piston locking mechanism which aids in the prevention of the accidental reuse of the syringe.

Source page: https://510kreport.com/device/K993609
Methodology: https://510kreport.com/methodology