Avacore Technologies, Inc. is one of 25717 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avacore Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RAPID THERMAL EXCHANGE SYSTEM, PALMO THERMOREGULATION INTERFACE ACCESSORY
2
Total
2
Cleared
0
Denied
Avacore Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Avacore Technologies, Inc. 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 - Avacore Technologies, Inc.
2 devices