Salter Labs, Arvin Facility is one of 16073 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Salter Labs, Arvin Facility - FDA 510(k) Cleared Devices
Recent clearances: SALTER LABS BUBBLE HUMIDIFIER (HIGH FLOW)
1
Total
1
Cleared
0
Denied
Salter Labs, Arvin Facility has 1 FDA 510(k) cleared medical devices. Based in Arvin, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Salter Labs, Arvin Facility Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Salter Labs, Arvin Facility
1 devices