# K973115: Arripro 35 ST/TV

- Pathway: 510(k) (Traditional)
- Applicant: Arnold & Richter Cine Technik
- Decided: Sep 2, 1997 after 13 days
- Product code: IXC (Illuminator, Radiographic-Film)
- Device class: 1
- Regulation: 21 CFR 892.1890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K971128 (1997). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K971128: Cap-35B Iii/Cine 275, Jamieson Film Co. (1997) Summary page 1.

## Indications for use
The device is used for the diagnosis and quantitative evaluation of 35 mm cine radiographic images, which originating from radiographic imaging like Angiography. The device contains a visible light source covered with a translucent front that is intended to be used to view medical cine radiographic images (CFR 21 part 892.1890). It also allows to be used for wall projection. The medical device is not part of a diagnostic x-ray system. The device may only be operated in cathlabs, lecture halls and doctors’ consulting rooms. The device is only for use by medical professionals.

Source page: https://510kreport.com/device/K973115
Methodology: https://510kreport.com/methodology