Anesthetic Gas Reclamation, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anesthetic Gas Reclamation, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Dynamic Gas Scavenging System 2 (DGSS - 2)
1
Total
1
Cleared
0
Denied
Anesthetic Gas Reclamation, Inc. has 1 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Anesthetic Gas Reclamation, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ceutical Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Anesthetic Gas Reclamation, Inc.
1 devices