# K980180: 2700 Sample Manager

- Pathway: 510(k) (Traditional)
- Applicant: Waters Corporation
- Decided: Feb 12, 1998 after 23 days
- Product code: JQW (Station, Pipetting And Diluting, For Clinical Use)
- Device class: 1
- Regulation: 21 CFR 862.2750
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Waters 2700 Sample Manager is designed for use in a clinical laboratory to manage sample injection for high throughput LC and LCMS applications. The 2700 Sample Manager automates sample aspiration and injection from microtiter plates, test tubes, Eppendorf tubes, or conventional autosampler vials. This product is intended for In Vitro Diagnostic Use.

Source page: https://510kreport.com/device/K980180
Methodology: https://510kreport.com/methodology