Halkey-Roberts Corp. is one of 25292 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Halkey-Roberts Corp. - FDA 510(k) Cleared Devices
Recent clearances: ROBERTSITE STOPCOCK, ROBERTSITE VIAL ADAPTER, MODEL 245700021
2
Total
2
Cleared
0
Denied
Halkey-Roberts Corp. has 2 FDA 510(k) cleared medical devices. Based in St. Petersburg, US.
Historical record: 2 cleared submissions from 2004 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Halkey-Roberts Corp. 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 - Halkey-Roberts Corp.
2 devices