# K991435: Aii-Pro 100 Plus and All-Pro 200

- Pathway: 510(k) (Traditional)
- Applicant: All-Pro Imaging Corp.
- Decided: May 20, 1999 after 24 days
- Product code: IXW (Processor, Radiographic-Film, Automatic)
- Device class: 2
- Regulation: 21 CFR 892.1900
- 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 All-Pro 100 Plus and All-Pro 200 are automatic x-ray film processors. They develop, fix wash and dry medical x-ray film. Properly processed x-ray films are available for reading by medical practitioners more rapidly and with more consistency than with manual processing.

Source page: https://510kreport.com/device/K991435
Methodology: https://510kreport.com/methodology