# K013614: Trojan Crystal Clear Liquid

- Pathway: 510(k) (Traditional)
- Applicant: Armkel, LLC
- Decided: Feb 1, 2002 after 88 days
- Product code: NUC (Lubricant, Personal)
- Device class: 2
- Regulation: 21 CFR 884.5300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K890863 (1989). 1 ancestor in all.
7 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K890863: Trojan for Women, Armkel, LLC (1989) Summary page 1.
- (no number) HeR® Lubricating Jelly: named in the summary without a submission number

## Most influential descendants
- K120751: Nirvana B Personal Lubricant (2012), 6 descendants of its own
- K181408: JO Classic Hybrid Personal Lubricant (2018), 4 descendants of its own
- K191480: Wet Water Based Personal Lubricant (additionally, branded as WET Platinum Houston, Elite Water-Based Hybrid) (2019), 3 descendants of its own
- K212000: Medley (2021), 1 descendant of its own
- K234099: Select Hybrid Personal Lubricant, and Select Pure Silicone Personal Lubricant (2024), 0 descendants of its own

## Indications for use
The TROJAN® CRYSTAL CLEAR Liquid is principally designed to help enhance the sexual experience by providing supplemental vaginal lubrication during sexual intercourse. The TROJAN® CRYSTAL CLEAR Liquid may be used with condoms. The TROJAN® CRYSTAL CLEAR Liquid patient lubricant is a device intended for medical purposes that is used to lubricate a body orifice to facilitate entry of a diagnostic or therapeutic device.

Source page: https://510kreport.com/device/K013614
Methodology: https://510kreport.com/methodology