Zcv ,Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zcv ,Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Zcv ,Inc. has 6 FDA 510(k) cleared medical devices. Based in Edison, US.
Historical record: 6 cleared submissions from 1999 to 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Zcv ,Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zcv ,Inc.
6 devices
Cleared
Feb 01, 2001
ZYNERGY Z3K BALLOON GUIDED PACING AND MONITORING CATHETER
Cardiovascular
21d
Cleared
Jan 08, 2001
ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER
Cardiovascular
139d
Cleared
Dec 20, 2000
Z2 BALLOON GUIDED PACING & PRESSURE MONITORING CATHETER, MODEL Z2-7-02-1-10-0
Cardiovascular
76d
Cleared
Dec 07, 2000
ZYNERGY FEATHERPACE TRANSVENOUS BIPOLAR CATHETER, MODEL 04-X-02-3-10-3
Cardiovascular
115d
Cleared
Apr 06, 2000
ZYNERGY ZOLUTION ELECTROPHYSIOLOGY CATHETER, MODEL Z50000
Cardiovascular
373d
Cleared
Sep 03, 1999
ZYNERGY LOCK-SURE SINGLE PASS DRAINAGE CATHETER, Z10005/7/9
Gastroenterology & Urology
184d