Cewal, Inc. Dba Premiere Enterprises is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cewal, Inc. Dba Premiere Enterprises - FDA 510(k) Cleared Devices
Recent clearances: Creme de La Femme Feminine Lubricant
1
Total
1
Cleared
0
Denied
Cewal, Inc. Dba Premiere Enterprises has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Cewal, Inc. Dba Premiere Enterprises Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Amin Talati Upadhye, Llp as regulatory consultant.
FDA 510(k) Regulatory Record - Cewal, Inc. Dba Premiere Enterprises
1 devices