# K042484: Nai Tech Products Medical Digital Recorder

- Pathway: 510(k) (Traditional)
- Applicant: Nai Technology Products
- Decided: Oct 20, 2004 after 37 days
- Product code: LMA (Digitizer, Image, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2030
- 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 NAI Tech Products Medical Digital Recorder is intended for use in Radiology to capture and digitize single or multiple video images and record them to removable media in the form of CD (Compact Disc) or DVD (Digital Video Disc).

Source page: https://510kreport.com/device/K042484
Methodology: https://510kreport.com/methodology