Grundler GmbH is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Grundler GmbH has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Grundler GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Grundler GmbH
1 devices