# K931297: GCA-7200A

- Pathway: 510(k) (Traditional)
- Applicant: Toshiba America Medical Systems, In.C
- Decided: Jul 27, 1993 after 134 days
- Product code: KPS (System, Tomography, Computed, Emission)
- Device class: 2
- Regulation: 21 CFR 892.1200
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K992992: Automatic Image Registration Software, Model Nsfu-050A (1999), 0 descendants of its own
- K960948: Scatter Correction Volume Software Model NSSC-020A (1996), 0 descendants of its own

## Recalls of this device
- May 31, 2004 · Not classified · Z-1059-04: Pinhole collimator defective.

Source page: https://510kreport.com/device/K931297
Methodology: https://510kreport.com/methodology