# K871202: Flashpak Container System

- Pathway: 510(k) (Traditional)
- Applicant: Performance Instruments Corp.
- Decided: May 29, 1987 after 65 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.
29 later devices descend from it; 5 cite it directly.
0 of 30 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
- K022978: Steritite Container with Flashtite Valve Plate (S) & Meditray Products (2003), 25 descendants of its own
- K053389: Aesculap Sterilcontainer System (2006), 12 descendants of its own
- K073168: Aesculap Primeline Container LTD. (2008), 9 descendants of its own
- K112671: Sterilcontainer System (2012), 7 descendants of its own
- K072563: Miltex Rigid Container Systems (2008), 7 descendants of its own

Source page: https://510kreport.com/device/K871202
Methodology: https://510kreport.com/methodology