# Intl. Cytobrush, Inc.

- Location (FDA's records): Hollywood, FL
- FDA decisions: 4 (1986–1990): 4 510(k) clearances
- Product codes: HHT (3), HFE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Excell Company, LLC: 1 (https://510kreport.com/company/excell)
- Kolplast CI SA: 1 (https://510kreport.com/company/kolplast-ci)
- Diamics, Inc.: 1 (https://510kreport.com/company/diamics)

## Its most-cited devices
- K861389: Pap Smear Kit (1986), cited by 3

## Recent decisions
- K897070: Endobrush (TM) Device; Omnibrush (Sep 10, 1990)
- K895675: Pap Smear Tray (Dec 11, 1989)
- K862322: Chlamydia Kit, STD Kit (Jul 7, 1986)
- K861389: Pap Smear Kit (May 2, 1986)

Source page: https://510kreport.com/company/intl-cytobrush