# K951552: Boston Contact Lens Case

- Pathway: 510(k) (Traditional)
- Applicant: Polymer Technology Corp.
- Decided: Jun 26, 1995 after 83 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
No predicates in its family tree.
5 later devices descend from it; 1 cites 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K962512: Boston Contact Lens Case (1996), 4 descendants of its own
- K974635: Paragon Lens Care (1998), 3 descendants of its own
- 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

Source page: https://510kreport.com/device/K951552
Methodology: https://510kreport.com/methodology