# K021752: FP (Hexafocon a)RGP Contact Lens Spherical/Asp (Hexafocon a)RGP Contact Lens Aspherical

- Pathway: 510(k) (Traditional)
- Applicant: Lucid Korea Co., Ltd.
- Decided: Oct 11, 2002 after 136 days
- Product code: HQD (Lens, Contact (Other Material) - Daily)
- Device class: 2
- Regulation: 21 CFR 886.5916
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K984436 (1999). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K000795: Rigid Gas Permeable Contact Lens, Polymer Technology (2000)
- K984436: PVS Basics, Paragon Vision Sciences (1999) Summary page 1.

## Indications for use
FP(hexafocon A) and ASP(hexafocon A) RGP Contact Lens are indicated for daily wear for the correction of refractive amptropia (myopia, hyperopia, astigmatism) in aphakic and not- aphakic persons with nondiseased eyes. The lens may be disinfected using a chemical disinfecting system only.

Source page: https://510kreport.com/device/K021752
Methodology: https://510kreport.com/methodology