# K981151: Opti-Free Supraclens Daily Protein Remover/Alcon Wetting, Soaking, Conditioning and Disinfecting Solution ID 84392

- Pathway: 510(k) (Traditional)
- Applicant: Alcon Laboratories
- Decided: Jun 22, 1998 after 84 days
- Product code: LPN (Accessories, Soft Lens Products)
- 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- P830071: Improved Soaclens, Alcon Laboratories. FDA lists this PMA only through its supplements; the earliest we hold is P830071/S002 (Dec 30, 1987). Summary page 2.

## Cited in the summary but kept off the family tree
- P82002: Alcon OPTI-FREE® SUPRACLENS® Daily Protein Remover. Number could not be read Summary page 2.

## Indications for use
OPTI-FREE® SUPRACLENS® Daily Protein Remover is indicated for use with clear and tinted, daily wear and extended wear soft (hydrophilic) contact lenses or rigid gas permeable (silicone acrylate fluorosilicone acrylate) lenses to simultaneously enzymatically clean them while they are being disinfected (soaked) in, OPTI-FREE® Rinsing, Disinfecting and Storage Solution, OPTI-ONE Multi-Purpose Solution, or OPTI-FREE® EXPRESS Multi-Purpose Solution or conditioned in OPTI-SOAK Conditioning Solution or Alcon Wetting, Soaking, Conditioning and Disinfecting Solution ID 84392. Use as recommended by your eye care practitioner. Alcon Wetting, Soaking, Conditioning and Disinfecting Solution ID 84392 is for the disinfection and conditioning after cleaning and rinsing of clear and tinted, daily and extended wear fluorosilicone acrylate and silicone acrylate rigid gas permeable lenses. Alcon Wetting, Soaking, Conditioning and Disinfecting Solution ID 84392 can also be used as a diluent for OPTI-FREE® SUPRACLENS® Daily Protein Remover.

Source page: https://510kreport.com/device/K981151
Methodology: https://510kreport.com/methodology