# K831425: MDT Chemitest See-Thru Bag

- Pathway: 510(k) (Traditional)
- Applicant: Kenpak Converters, Inc.
- Decided: Jun 2, 1983 after 30 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K152058: Tyvek Sterilization Pouches with Chevron Seal (2015), 2 descendants of its own
- K200336: Tyvek Sterilization Pouches with Chevron Seal (2020), 0 descendants of its own
- K170429: Tyvek Sterilization Pouches with Chevron Seal (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K831425
Methodology: https://510kreport.com/methodology