Medical Device Manufacturer · US , Mchenry , IL

Med-West, Inc. - FDA 510(k) Cleared Devices

11 submissions · 8 cleared · Since 1983

Total

Cleared

Denied

Med-West, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1983 to 1988. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Med-West, Inc. Filter by specialty or product code using the sidebar.

Med-West, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Med-West, Inc.

11 devices

1-11 of 11

Cleared May 31, 1988

CONTRAST INJECTION DEVICE

K880877 · DXT

Cardiovascular · 91d

Cleared Mar 17, 1988

POWER TOILET ELEVATOR

K880398 · INO

Physical Medicine · 48d

Cleared Dec 18, 1987

MWI 400 WOUND DRESSING

K874470 · NAD

General & Plastic Surgery · 46d

ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7

K854612 · LFK

Gastroenterology & Urology · 46d

Cleared Jun 12, 1985

MNI 400 INJECTION CAPS

K852162 · LFJ

Gastroenterology & Urology · 23d

Cleared Jun 14, 1984

MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN

K842342

Gastroenterology & Urology

Cleared Aug 12, 1983

CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI

K832124 · DWF

Cardiovascular · 43d

Cleared Jul 07, 1983

TEFLON FEMORAL CATHETER MWI 100,10 &

K831828 · LFK

Gastroenterology & Urology · 30d

Cleared Jun 03, 1983

SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS

K831401 · FIQ

Gastroenterology & Urology · 32d

Cleared Jun 03, 1983

SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260

K831440 · FIQ

Gastroenterology & Urology · 29d

Med-West, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Med-West, Inc.

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