# K924334: Cidex Formula 7* Long-Life Activated Dialdehyde

- Pathway: 510(k) (Traditional)
- Applicant: Johnson & Johnson Medical, Inc.
- Decided: Mar 29, 1994 after 579 days
- Product code: MED (Sterilant, Medical Devices)
- Device class: 2
- Regulation: 21 CFR 880.6885
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
16 later devices descend from it; 3 cite it directly.
0 of 17 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
- K972708: Endo-Spor Plus / Hyprocide (1999), 7 descendants of its own
- K970230: Sporox (1997), 7 descendants of its own
- K013280: Sterilox Liquid Chemical Sterilant System (2002), 6 descendants of its own
- K090036: System 1.5 Sterile Processing System (2010), 4 descendants of its own
- K103059: Trophon (2011), 3 descendants of its own

Source page: https://510kreport.com/device/K924334
Methodology: https://510kreport.com/methodology