Erka Kallmeyer Medizintechnik GmbH is one of 387 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Erka Kallmeyer Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: ERKA. PERFECT-ANEROID
1
Total
1
Cleared
0
Denied
Erka Kallmeyer Medizintechnik GmbH has 1 FDA 510(k) cleared medical devices. Based in Bad Toelz, Bavaria, DE.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Erka Kallmeyer Medizintechnik 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 - Erka Kallmeyer Medizintechnik GmbH
1 devices