# K894069: Abbott Commander Flexible Pipetting Center

- Pathway: 510(k) (Traditional)
- Applicant: Abbott Laboratories
- Decided: Aug 21, 1989 after 74 days
- Product code: JQW (Station, Pipetting And Diluting, For Clinical Use)
- Device class: 1
- Regulation: 21 CFR 862.2750
- Recalls of this device: 1 (0 Class I)
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Dec 2, 2003 · Not classified · Z-0297-04: The Operations Manual has the wrong Farenheit temperature range listed (102-122) instead of (104-122) for the preparation of the Terg-A-Zyme solution used to clean pipettes of the Abbott Commander Fle

Source page: https://510kreport.com/device/K894069
Methodology: https://510kreport.com/methodology