# K962934: Airperm (Siflufocon a) Rigid Gas Permeable Multifocal Contact Lenses for Daily Wear

- Pathway: 510(k) (Traditional)
- Applicant: Airperm, Inc.
- Decided: Aug 27, 1996 after 29 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
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)
- None. The FDA summary names no predicate by number.

## Indications for use
The AIRPERM (siflufocon A) Rigid Gas Permeable Spherical, Aspherical, Toric and Multifocal Contact Lens is indicated for daily wear for the correction of refractive ametropia (myopia, hyperopia, astigmatism and presbyopia) in non-aphakic persons with non-diseased eyes. The lens may be disinfected using a chemical disinfection system only.

Source page: https://510kreport.com/device/K962934
Methodology: https://510kreport.com/methodology