# K022086: Aim-V (R) Medium, Model 087-0112

- Pathway: 510(k) (Traditional)
- Applicant: Invitrogen Corporation
- Decided: Dec 23, 2002 after 179 days
- Product code: NDS (Media, Culture, Ex Vivo, Tissue And Cell)
- Device class: 2
- Regulation: 21 CFR 876.5885
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to DEN000008 (2001). 1 ancestor in all.
7 later devices descend from it; 4 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- DEN000008: Dulbecco's Modified Eagle Medium (Dmem), Life Technologies, Inc. (2001). Our reading of the summary gave K001447, which is not in FDA’s 510(k) list. The device the summary names is FDA’s De Novo DEN000008, Dulbecco's Modified Eagle Medium (Dmem) (Life Technologies, Inc.), granted Feb 16, 2001; older De Novo requests were first filed under a 510(k) number, so this links to the grant.

## Most influential descendants
- K100616: Knockout SR Medium, Knockout SR Xenofree Medium Model 10828, 12618 (2010), 3 descendants of its own
- K201789: CT-Stor (2021), 1 descendant of its own
- K103302: Stempro MSC SFM (2011), 1 descendant of its own
- K232543: MSC SFM (2024), 0 descendants of its own
- K240247: “MoFi” Cell Culture Basal Medium (2024), 0 descendants of its own

## Recalls of this device
- May 10, 2018 · Class II · Z-2543-2018: It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging into outer no

## Indications for use
AIM-V@ is a liquid tissue culture media product intended for human ex vivo tissue and cell culture processing applications.

Source page: https://510kreport.com/device/K022086
Methodology: https://510kreport.com/methodology