# K900432: Model #M8 Electronic Sterilizer

- Pathway: 510(k) (Traditional)
- Applicant: Midmark Corp.
- Decided: Jul 27, 1990 after 178 days
- Product code: FLE (Sterilizer, Steam)
- Device class: 2
- Regulation: 21 CFR 880.6880
- 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
- K962903: Prestige Medical Series 2100 Clinical Autoclave (1998), 1 descendant of its own
- K063681: Tecno-Gaz Andromeda Vacuum CS Autoclave (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K900432
Methodology: https://510kreport.com/methodology