# K082855: Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses

- Pathway: 510(k) (Traditional)
- Applicant: Menicon Co, Ltd.
- Decided: Mar 9, 2010 after 526 days
- Product code: MRC (Products, Contact Lens Care, Rigid Gas Permeable)
- Device class: 2
- Regulation: 21 CFR 886.5918
- 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 K002140 (2000). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002140: Menicon Progent Remover, Menicon Co, Ltd. (2000) Summary page 1.
- P820069: Boston Lens (R) Cleaner, Polymer Technology Corp.. FDA lists this PMA only through its supplements; the earliest we hold is P820069/S001 (Mar 16, 1984). Summary page 1.

## Most influential descendants
- K122273: Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lens (2013), 1 descendant of its own
- K130285: Progent Large Diameter Contact Lens Case for Rigid Gas Permeable Lens (2013), 0 descendants of its own

## Indications for use
Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses, when used as directed, cleans and removes protein deposits from fluorosilicone acrylate rigid gas permeable contact lenses.

Source page: https://510kreport.com/device/K082855
Methodology: https://510kreport.com/methodology