# K181566: Nutrifill

- Pathway: 510(k) (Traditional)
- Applicant: Contamac, Ltd.
- Decided: Oct 22, 2018 after 130 days
- Product code: MRC (Products, Contact Lens Care, Rigid Gas Permeable)
- Device class: 2
- Regulation: 21 CFR 886.5918
- Recalls of this device: 2 (0 Class I)
- 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.

## Recalls of this device
- May 15, 2025 · Class II · Z-1956-2025: Contact lens insertion solution may lack sterility.
- Jul 27, 2021 · Class II · Z-0030-2022: Contact lens solution may contain foreign material

Source page: https://510kreport.com/device/K181566
Methodology: https://510kreport.com/methodology