# K852069: Mecta Ect Device Models SR & JR

- Pathway: 510(k) (Traditional)
- Applicant: Mecta Corp.
- Decided: Aug 9, 1985 after 91 days
- Product code: QGH (Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder)
- Device class: 2
- Regulation: 21 CFR 882.5940
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices 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.

## Most influential descendants
- K960754: Spectrum 5000 Q, 5000 M, 4000 Q, 4000 M (1996), 1 descendant of its own
- K965070: Spectrum  5000 Q, 5000Q,M,4000 Q, 4000 M. (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K852069
Methodology: https://510kreport.com/methodology