RQMIS, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
RQMIS, Inc. - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
RQMIS, Inc. has 0 FDA 510(k) cleared medical devices. Based in Amesbury, US.
Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by RQMIS, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - RQMIS, Inc.
1 devices