# K912073: Polaroid Helios Laser Imager

- Pathway: 510(k) (Traditional)
- Applicant: Polaroid Medical Corp.
- Decided: Aug 28, 1991 after 110 days
- Product code: LMC (Camera, Multi Format, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2040
- Recalls of this device: none
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K972660: Raven Dry Printer (1997), 0 descendants of its own
- K973028: Helios Laser Imager 1417 (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K912073
Methodology: https://510kreport.com/methodology