# K932652: Tri-Med Paracentesis Tray

- Pathway: 510(k) (Traditional)
- Applicant: Tri-Med Specialties, Inc.
- Decided: Nov 24, 1993 after 175 days
- Product code: LRO (General Surgery Tray)
- Device class: 2
- Regulation: 21 CFR 878.4370
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K960456: Denver Paracentesis Needle (60-1200) Denver Paracentesis Needle with Drainage Line (60-1100) Denver Paracentesis Tray (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K932652
Methodology: https://510kreport.com/methodology