Medimex Holfeld GmbH & Co. is one of 8702 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medimex Holfeld GmbH & Co. - FDA 510(k) Cleared Devices
Recent clearances: EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS
1
Total
0
Cleared
0
Denied
Medimex Holfeld GmbH & Co. has 0 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 0 cleared submissions from 1999 to 1999. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Medimex Holfeld GmbH & Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medimex Holfeld GmbH & Co.
1 devices