# Curative Medical, Inc.

- Location (FDA's records): Fulshear, TX
- FDA decisions: 6 (2012–2015): 6 510(k) clearances
- Product codes: BZD (5), DQY (1)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 3 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Respironics, Inc.: 2 (https://510kreport.com/company/respironics)
- Resmed, Ltd.: 1 (https://510kreport.com/company/resmed)
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)

## Its most-cited devices
- K123897: K Series Cpap Systems (2013), cited by 2
- K120285: K Series Cpap System with Heated Humidifer (2012), cited by 1

## Recent decisions
- K141354: Navajo Pta Balloon Dilatation Catheter (Jan 30, 2015)
- K130828: K Series Cpap Systems (Jan 13, 2014)
- K131702: K Series Cpap Systems (Dec 6, 2013)
- K130663: BESTFIT2 Nasal Mask (Sep 27, 2013)
- K123897: K Series Cpap Systems (Mar 13, 2013)
- K120285: K Series Cpap System with Heated Humidifer (Jul 2, 2012)

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