# K120821: Llics (TM) Laparascopic Lens Internal Cleaning System

- Pathway: 510(k) (Traditional)
- Applicant: Misder, LLC
- Decided: May 11, 2012 after 53 days
- Product code: OCT (Anti Fog Solution And Accessories, Endoscopy)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K904871 (1991). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K974454: Clearfield Anti-Fog Sterile Wipe, Product Number 300-004, Tucson Medical Corp. (1997) Summary page 4.

## Cited in the summary but kept off the family tree
- K062779: Defogging Heated Endoscope Lens Protector (Dhelp); Defogging Endoscope Lens Protector (Delp), New Wave Surgical Corporation (2006). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Indications for use
The LLICS™ is indicated for use in laparoscopic surgeries to clean the laparoscope lens within the surgical cavity, preventing temperature changes associated with lens fogging.

Source page: https://510kreport.com/device/K120821
Methodology: https://510kreport.com/methodology