Elm Tree Medical, Inc. is one of 19028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Elm Tree Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DilaCheck Nitrile Powder Free Examination Glove, (Sterile)
1
Total
1
Cleared
0
Denied
Elm Tree Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Elm Tree Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedic, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Elm Tree Medical, Inc.
1 devices