# Ansley Medical Products, Inc.

- Location (FDA's records): Dallas, TX
- FDA decisions: 5 (1992–1993): 5 510(k) clearances
- Product codes: KMK (3), KKX (1), LYU (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K932857: Abdominal Fluid Control Pouch, 203-301-S;Etc. (Sep 13, 1993)
- K925290: Catalog Number 111  (Faceshield) (Jul 23, 1993)
- K924568: Tube, Lead, and Cord Holder NO. 102 (Nov 23, 1992)
- K924566: Restraint, Protective N0. 103 (Nov 23, 1992)
- K924567: Foley Catheter Tube Holder NO. 101 (Nov 23, 1992)

Source page: https://510kreport.com/company/ansley-medical-products