# K040865: Aesculap Sterrad 100S Compatable Sterilcontainer

- Pathway: 510(k) (Traditional)
- Applicant: Aesculap
- Decided: Dec 6, 2004 after 248 days
- Product code: FRG (Wrap, Sterilization)
- Device class: 2
- Regulation: 21 CFR 880.6850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 2 cite it directly.
0 of 11 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) Aesculap Sterilcontainers: named in the summary without a submission number
- (no number) Allegiance Healthcare (Genesis) sterilization containers: named in the summary without a submission number
- (no number) Case Medical (SteriTite) sterilization containers: named in the summary without a submission number

## Most influential descendants
- K093493: Aesculap Sterilcontainer S (2010), 4 descendants of its own
- K093649: Aesculap Sterilcontainer S (2010), 4 descendants of its own
- K151242: SterilContainer S (2015), 2 descendants of its own
- K162815: SterilContainer S System (2017), 1 descendant of its own
- K110682: Steritite Container System & Meditray Products (2011), 1 descendant of its own

## Indications for use
The Aesculap Sterilcontainer is a reusable sterilization container system intended to be used to enclose another medical device that is to be sterilized by a healthcare provider. It is intended to allow sterilization of the enclosed device and also maintain sterility of the enclosed device until used. This container system is compatible for use with the Sterrad 100S.

Source page: https://510kreport.com/device/K040865
Methodology: https://510kreport.com/methodology