# K990266: Micromedical 12 Lead Simultaneous Cable

- Pathway: 510(k) (Special)
- Applicant: Micromedical Industries, Ltd.
- Decided: Feb 2, 1999 after 5 days
- Product code: LOS
- 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.
3 later devices descend from it; 2 cite 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)
- None. The FDA summary names its predicate without a number.
- (no number) 12 Lead Simultaneous Cable: named in the summary without a submission number

## Most influential descendants
- K102378: Vectraplexecg System with Vectraplexami (2011), 2 descendants of its own
- K173952: Universal SmartECG (2018), 1 descendant of its own
- K232035: Impala (2024), 0 descendants of its own

## Recalls of this device
- Feb 16, 2012 · Not classified · Z-1315-2012: QRS Diagnostic has initiated a recall involving Universal ECG 12 Lead IEC ECG Devices. This recall has been initiated because the chest lead wires on these devices may have been improperly labeled. In

## Indications for use
The 12 Lead Simultaneous Cable is used to acquire a patient’s ECG via 10 leads connected to a patient’s chest. It converts the ECG signal into a digital format and transfers this information to a Micromedical monitor or software system using a proprietary digital data transfer protocol.

Source page: https://510kreport.com/device/K990266
Methodology: https://510kreport.com/methodology