Retrax Safety Systems, Inc. is one of 26084 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Retrax Safety Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RETRAX RETRACTING NEEDLE SYRINGE, SIZE 3CC
1
Total
1
Cleared
0
Denied
Retrax Safety Systems, Inc. has 1 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Retrax Safety Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Retrax Safety Systems, Inc.
1 devices