# K993962: Pensil Trauma, Model WWS6100

- Pathway: 510(k) (Traditional)
- Applicant: Wuestec Medical, Inc.
- Decided: Dec 21, 1999 after 57 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Pensil Trauma is a wall-mounted radiographic cassette holder device that is a support intended to hold and position radiographic cassettes for a radiographic exposure for medical use.

Source page: https://510kreport.com/device/K993962
Methodology: https://510kreport.com/methodology