Rmds, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rmds, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Rmds, Inc. has 4 FDA 510(k) cleared medical devices. Based in Vancouver, US.
Historical record: 4 cleared submissions from 1997 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Rmds, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rmds, Inc.
4 devices
Cleared
Dec 11, 1997
FAVP: FEMORAL ARTERY VASCULAR PAD - MODEL NUMBER PAD2EK-01, PAD2EK-2X,...
Cardiovascular
385d
Cleared
Nov 25, 1997
FAVC-HH: FEMORAL ARTERY VASCULAR CLAMP-HAND HELD: 1/2 & 3 POUNDS...
Cardiovascular
90d
Cleared
Aug 08, 1997
FAVC-M: FEMORAL ARTERY VASCULAR CLAMP-MOBILE (MODEL M100-M200) FAVC-M FEMORAL...
Cardiovascular
217d
Cleared
Feb 03, 1997
FAVC: FEMORAL ARTERY VASCULAR CLAMP - MODEL NUMBER RMDS 1000-15, RMDS...
Cardiovascular
74d