# K925816: Sharps Containment System

- Pathway: 510(k) (Traditional)
- Applicant: Post Medical, Inc.
- Decided: Apr 29, 1994 after 528 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K982781: Demolizer #47 One-Gallon Point of Generation Sharps Container (1998), 3 descendants of its own
- K131708: Bwcsh-1 Sharps Container (2014), 1 descendant of its own
- K182235: OnSite Waste Sharps Container (2019), 0 descendants of its own
- K123807: Sharpscan (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K925816
Methodology: https://510kreport.com/methodology