Van-Tec, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Van-Tec, Inc. - FDA 510(k) Cleared Devices
52
Total
52
Cleared
0
Denied
Van-Tec, Inc. has 52 FDA 510(k) cleared gastroenterology & urology devices. Based in Walker, US.
Historical record: 52 cleared submissions from 1982 to 1988.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Van-Tec, Inc.
52 devices
Cleared
Mar 02, 1988
BERGER PROSTATE CULTURE CYTOLOGY BRUSH
Gastroenterology & Urology
50d
Cleared
Mar 02, 1988
VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUP
Gastroenterology & Urology
50d
Cleared
Mar 02, 1988
VAN-TEC AUTO BIOPSY NEEDLE
Gastroenterology & Urology
50d
Cleared
Mar 02, 1988
VAN-TEC BLADDER EVACUATOR
Gastroenterology & Urology
50d
Cleared
Feb 29, 1988
VAN-TEC ENDOPYELOTOMY KNIFE
General & Plastic Surgery
48d
Cleared
Feb 11, 1988
VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER
Gastroenterology & Urology
125d
Cleared
Jun 17, 1987
VAN-TEC REUSABLE HELICAL STONE BASKET
Gastroenterology & Urology
42d
Cleared
Jun 17, 1987
HELICAL STONE BASKET (DISPOSABLE)
Gastroenterology & Urology
42d
Cleared
Mar 30, 1987
VAN-TEC PUMPING SYSTEM
Gastroenterology & Urology
48d
Cleared
Mar 30, 1987
VAN-TEC MODULAR FLEXIBLE CYSTOURETHROSCOPE
Gastroenterology & Urology
39d
Cleared
Mar 30, 1987
VAN-TEC SEGURA STONE BASKET W/PROTECTIVE SHEATH
Gastroenterology & Urology
39d
Cleared
Mar 25, 1987
KAMINSKY COMBINATION STENT & INJECTION CATHETER
Gastroenterology & Urology
85d
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