# K974635: Paragon Lens Care

- Pathway: 510(k) (Traditional)
- Applicant: Paragon Vision Sciences
- Decided: Feb 4, 1998 after 54 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: 2 generations back to K951552 (1995). 2 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962512: Boston Contact Lens Case, Polymer Technology Div. Wilmington Partners, L.P. (1996) Summary page 1.

## Most influential descendants
- K993486: Paragon Lens Carrier (1999), 1 descendant of its own
- K993487: Paragon Lens Vial (1999), 1 descendant of its own
- K040914: Polyvial/Polypak, Contact Lens Case and Storage System Container for Ophthalmics (2004), 0 descendants of its own

## Indications for use
The Paragon Contact Lens Case is indicated for storage of rigid gas permeable and hard contact lenses during chemical disinfection

Source page: https://510kreport.com/device/K974635
Methodology: https://510kreport.com/methodology