Medical Device Manufacturer · US , Mchenry , IL

Venusa , Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1981

8

Total

8

Cleared

0

Denied

Venusa , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1981 to 2000. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Venusa , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Venusa , Ltd.

8 devices

1-8 of 8

Cleared Mar 03, 2000

VENUSA, LTD. EXTENSION SET WITH FILTER

General Hospital · 64d

Cleared Jul 28, 1998

HUBER NEEDLE INFUSION SET MODEL #20G01 & Y-SITE MODEL #20G01Y

General Hospital · 76d

Cleared Jun 21, 1991

BERLEX BOLUS/INFUSION(TM) INTRAVENOUS ADMIN SET

Radiology · 196d

Cleared Sep 05, 1985

ENTERAL FEEDING BAG, 1000 ML, & TUBING SET

Gastroenterology & Urology · 121d

Cleared Oct 31, 1984

FLU VEN I.V. SET 0153-C PERMA-SET

General Hospital · 42d

Cleared Aug 17, 1984

General Hospital · 85d

Cleared Nov 06, 1981

FLUVEN SETS (EXT-1, EXT-2, EXT-3, EXT-4)

General Hospital · 14d

Cleared Aug 03, 1981

FLU VEN I.V. SETS

General Hospital · 33d