Atmos, Inc. is one of 23498 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atmos, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ATMOS E 201 THORAX AND ATMOS S 201 THORAX, ATMOS S041 WOUND, ATMOS C361/C451 SUCTION PUMP
3
Total
3
Cleared
0
Denied
Atmos, Inc. has 3 FDA 510(k) cleared medical devices. Based in Denton, US.
Historical record: 3 cleared submissions from 2009 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Atmos, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Atmos, Inc.
3 devices