# K131783: Polaroid Contactspod

- Pathway: 510(k) (Traditional)
- Applicant: Viopti, Ltd.
- Decided: Feb 21, 2014 after 249 days
- Product code: LRX (Case, Contact Lens)
- Device class: 2
- Regulation: 21 CFR 886.5928
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K920064 (1992). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130753: Standard Contact Lens Case; Flip N Slide Contact Lens Case, Watchdog Group, LC (2013) Summary page 2.

## Indications for use
The Contactspod is a sterile single-use temporary storage case and contains multipurpose contact lens solution for use with soft contact lenses. It is not a replacement for your normal contact lens rub and rinse cleaning and disinfecting care regimen. It is a clear solution and should not be used if cloudy or discolored. Use for storage during chemical disinfection only. DO NOT USE WITH HEAT.

Source page: https://510kreport.com/device/K131783
Methodology: https://510kreport.com/methodology