# K982824: X-Ray Timer Model I.E.D. 7888 I.D. 7881 and B764ID

- Pathway: 510(k) (Traditional)
- Applicant: I.E.D., Inc.
- Decided: Oct 29, 1998 after 79 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
To control the X-Ray on time exposure

Source page: https://510kreport.com/device/K982824
Methodology: https://510kreport.com/methodology