# K992317: Autospect Plus with Instill Motion Correction

- Pathway: 510(k) (Traditional)
- Applicant: Adac Laboratories
- Decided: Oct 1, 1999 after 84 days
- Product code: KPS (System, Tomography, Computed, Emission)
- Device class: 2
- Regulation: 21 CFR 892.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
22 later devices descend from it; 4 cite it directly.
0 of 23 devices 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) SMV Statis™: named in the summary without a submission number
- (no number) SMV MyoSPECT with ReOrient Express: named in the summary without a submission number

## Most influential descendants
- K042903: Autospecs (2004), 13 descendants of its own
- K090403: Autospect (2009), 12 descendants of its own
- K111336: EBW NM 2.0 (2011), 9 descendants of its own
- K162955: Multi-Modality Tumor Tracking (MMTT) application (2016), 5 descendants of its own
- K071503: System, Tomography, Computed Emission (2007), 5 descendants of its own

## Indications for use
The AutoSPECT Plus with InStill Motion Correction option to the ADAC Gamma Camera Systems produces images which depict anatomical density of the patient. This system is intended to provide enhancements of gamma camera emission images by automating previously manual image processing functions and providing manual and automated motion correction.

Source page: https://510kreport.com/device/K992317
Methodology: https://510kreport.com/methodology