# K792558: Container System

- Pathway: 510(k) (Traditional)
- Applicant: Aesculap Instruments Corp.
- Decided: Dec 27, 1979 after 15 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.
16 later devices descend from it; 7 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
- K053389: Aesculap Sterilcontainer System (2006), 12 descendants of its own
- K041623: Reusable Sterilcontainer Filter Model #JK090 (2004), 10 descendants of its own
- K073168: Aesculap Primeline Container LTD. (2008), 9 descendants of its own
- K112671: Sterilcontainer System (2012), 7 descendants of its own
- K192056: JJ Series Container System (2020), 5 descendants of its own

Source page: https://510kreport.com/device/K792558
Methodology: https://510kreport.com/methodology