# Atmos Medizintechnik GmbH & Co. KG

- Location (FDA's records): Lenzkirch, DE
- FDA decisions: 2 (2023–2025): 2 510(k) clearances
- Product codes: EOB (1), BTA (1)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- Schoelly Fiberoptic GmbH: 1 (https://510kreport.com/company/schoelly-fiberoptic)
- Atmos, Inc.: 1 (https://510kreport.com/company/atmos)

## Recent decisions
- K241799: ATMOS C 051 Thorax (317.0200.0); Secretion canister 800ml (317.1300.0); Hose system (312.1177.0); Hose system with connector small (312.1206.0); Hose system with connector medium (312.1207.0); Hose system with connector large (312.1208.0); Hose system with Y-connector medium (312.1209.0); Hose system with Y-connector large (312.1210.0); Universal bracket for ATMOS C 051 Thorax (316.0200.0); Bracket for ATMOS C 051 Thorax - Standard rail (317.1160.0); Charger Storage for bracket ATMOS C (Mar 7, 2025)
- K232015: ATMOS Scope (507.7000.0); ATMOS Scope Pro (507.7050.0); ATMOS Scope iPrime (507.7060.0) (Aug 3, 2023)

Source page: https://510kreport.com/company/atmos-medizintechnik