# K962265: MLX Microtiter Plate Luminometer

- Pathway: 510(k) (Traditional)
- Applicant: Dynatech Laboratories, Inc.
- Decided: Jul 25, 1996 after 43 days
- Product code: JSE (Culture Media, Multiple Biochemical Test)
- Device class: 1
- Regulation: 21 CFR 866.2320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K915896 (1992). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K923456: Microlite Microtiter Plate Luminometer ML3000, Dynatech Laboratories, Inc. (1992) Summary page 1.
- K915896: Microlite Microtiter Plate Luminometer ML2250/Modi, Dynatech Laboratories, Inc. (1992) Summary page 1.

## Most influential descendants
- K980120: Digene DML 2000 Microplate Luminometer (1998), 0 descendants of its own

## Indications for use
The MLX measures the light emitted from bioluminescent and chemiluminescent reactions samples, performs defined test protocols and allows selection of various forms of output formats of the test results.

Source page: https://510kreport.com/device/K962265
Methodology: https://510kreport.com/methodology