# Atmos, Inc.

- Location (FDA's records): Allentown, PA
- FDA decisions: 3 (2009–2011): 3 510(k) clearances
- Product codes: BTA (2), OMP (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (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
- Blue Sky Medical Group Incorporated: 1 (https://510kreport.com/company/blue-sky-medical-group)
- Medela AG: 1 (https://510kreport.com/company/medela)
- Atrium Medical Corp.: 1 (https://510kreport.com/company/atrium-medical)
- Nouvag AG: 1 (https://510kreport.com/company/nouvag)

## Firms that cite its devices most
- Wound RX Medical, LLC: 1 (https://510kreport.com/company/wound-rx-medical)
- Atmos Medizintechnik GmbH & Co. KG: 1 (https://510kreport.com/company/atmos-medizintechnik)

## Its most-cited devices
- K090130: Atmos S041 Wound (2009), cited by 1
- K103042: Atmos E 201 Thorax and Atmos S 201 Thorax (2011), cited by 1

## Recent decisions
- K103042: Atmos E 201 Thorax and Atmos S 201 Thorax (Apr 15, 2011)
- K090130: Atmos S041 Wound (Apr 2, 2009)
- K090445: Atmos C361/C451 Suction Pump (Feb 27, 2009)

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