# K792712: Para-Pak (C&S)

- Pathway: 510(k) (Traditional)
- Applicant: Meridian Diagnostics, Inc.
- Decided: Jan 17, 1980 after 21 days
- Product code: JSM (Culture Media, Non-Propagating Transport)
- Device class: 1
- Regulation: 21 CFR 866.2390
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K150887: Para-Fix C&S Medium (2015), 0 descendants of its own
- K141506: MCC Para-Fix CARY BLAIR MEDIUM (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K792712
Methodology: https://510kreport.com/methodology