# Meditera Tibbi Malzeme San VE Tic AS

- Location (FDA's records): Izmir, TR
- FDA decisions: 3 (2020–2021): 3 510(k) clearances
- Product codes: CBP (1), CAH (1), CCK (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Intersurgical, Inc.: 1 (https://510kreport.com/company/intersurgical)
- Zhejiang Haisheng Medical Device Co., Ltd.: 1 (https://510kreport.com/company/zhejiang-haisheng-medical-device)
- Vyaire Medical, Inc.: 1 (https://510kreport.com/company/vyaire-medical)

## Firms that cite its devices most
- Passy-Muir, Inc.: 1 (https://510kreport.com/company/passy-muir)

## Its most-cited devices
- K192713: Altera Filter and HME/Filter (2020), cited by 1

## Recent decisions
- K210992: Altech® Exhalation Valve (Single Limb and Dual Limb) (Dec 23, 2021)
- K192713: Altera Filter and HME/Filter (Mar 16, 2020)
- K192563: Altera gas Sampling Lines (Jan 17, 2020)

Source page: https://510kreport.com/company/meditera-tibbi-malzeme-san-ve-tic
