# K200228: ClearCam System

- Pathway: 510(k) (Traditional)
- Applicant: Clearcam, LLC
- Decided: Feb 19, 2020 after 20 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- 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: 7 generations back to K904871 (1991). 22 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170103: Laparoscope Lens Shield Device (LENS), Medeon Biodesign, Inc. (2017) Summary page 4.

## Most influential descendants
- K241796: TroCare TroKit Laparoscope Lens Wiper (CP000626) (2024), 2 descendants of its own
- K253994: TroKit Laparoscope Lens Wiper (2026), 0 descendants of its own
- K260089: TL-10 Laparoscopic Scope Cleaner (2026), 0 descendants of its own

## Indications for use
The ClearCam System is indicated to provide lens clearing during laparoscopic procedures

Source page: https://510kreport.com/device/K200228
Methodology: https://510kreport.com/methodology