# K973239: Dicom 3.0 Software Version 2.0

- Pathway: 510(k) (Traditional)
- Applicant: Adac Laboratories
- Decided: Nov 26, 1997 after 90 days
- Product code: LMD (System, Digital Image Communications, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2020
- 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. The FDA summary names its predicate without a number.
- (no number) Cemax Vipstation: named in the summary without a submission number
- (no number) Avp Pacspro 640: named in the summary without a submission number

## Indications for use
DICOM 3.0 Software Version 2.0 is intended to provide communication and data interchange between multi-modality medical imaging devices, while maintaining the integrity of the image data.

Source page: https://510kreport.com/device/K973239
Methodology: https://510kreport.com/methodology