# K093649: Aesculap Sterilcontainer S

- Pathway: 510(k) (Traditional)
- Applicant: Aesculap
- Decided: May 11, 2010 after 167 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
Longest line of descent: 1 generation back to K040865 (2004). 1 ancestor in all.
4 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040865: Aesculap Sterrad 100S Compatable Sterilcontainer, Aesculap (2004) Summary page 1.

## Most influential descendants
- K151242: SterilContainer S (2015), 2 descendants of its own
- K162815: SterilContainer S System (2017), 1 descendant of its own
- K193582: SterilContainer S2 System (2020), 0 descendants of its own
- K143729: SterilContainer S (2015), 0 descendants of its own

## Indications for use
The Aesculap Sterilcontainer S 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 V-PRO 1 and V-PRO Plus Systems. The Sterilcontainer S is recommended for surface and lumens: * 1mm internal diameter and < 125 mm in length * 2mm internal diameter and < 250 mm in length * 3mm internal diameter and < 400 mm in length Lumen Cycle - The maximum number of lumens per load is 20 lumens. The attached table identifies which Sterilcontainer S may be sterilized in the V-PRO 1 and V-PRO Plus Systems.

Source page: https://510kreport.com/device/K093649
Methodology: https://510kreport.com/methodology