# Cheen Houng Ent. Co., Ltd.

- Location (FDA's records): Taipei (Shulin), TW
- FDA decisions: 6 (1997–2013): 6 510(k) clearances
- Product codes: BTM (2), CBP (1), BYI (1), KGB (1), BYE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Neoforce Group, Inc.: 1 (https://510kreport.com/company/neoforce-group)

## Its most-cited devices
- K981415: 0-20 CM H20 Peep Valve (1998), cited by 1

## Recent decisions
- K121587: Breath Shake (Nov 22, 2013)
- K021390: PMX Compact Resucitator (Oct 4, 2002)
- K003927: Y2000 Manual Resuscitator, Model RUGU01/RUG02 and RUGH01/RUGH02 (Jun 26, 2001)
- K010191: Y2000 Pocket Rescue (Mar 14, 2001)
- K981415: 0-20 CM H20 Peep Valve (Jul 14, 1998)
- K970688: Pocket Rescue (Sep 26, 1997)

Source page: https://510kreport.com/company/cheen-houng-ent