Vomed Volzer Medizintechnik GmbH & Co. is one of 141 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Vomed Volzer Medizintechnik GmbH & Co. - FDA 510(k) Cleared Devices
Recent clearances: VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000, VOMED PERIPHERAL VASCULAR ACCESSORIES, MODELS 1010 XXX-7090 XXX & 9006 XXX-9011 XXX, VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES
3
Total
3
Cleared
0
Denied
Vomed Volzer Medizintechnik GmbH & Co. has 3 FDA 510(k) cleared medical devices. Based in Amsterdam, Nh, NL.
Historical record: 3 cleared submissions from 2002 to 2002.
Browse the FDA 510(k) cleared devices submitted by Vomed Volzer Medizintechnik GmbH & Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vomed Volzer Medizintechnik GmbH & Co.
3 devices
Cleared
Dec 10, 2002
VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000
Gastroenterology & Urology
90d
Cleared
Oct 04, 2002
VOMED PERIPHERAL VASCULAR ACCESSORIES, MODELS 1010 XXX-7090 XXX & 9006...
Cardiovascular
84d
Cleared
Sep 19, 2002
VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES
Obstetrics & Gynecology
73d