Medical Device Manufacturer · US , Mchenry , IL

Mediflex Intl. - FDA 510(k) Cleared Devices

9 submissions · 8 cleared · Since 1984

Total

Cleared

Denied

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

Historical record: 8 cleared submissions from 1984 to 1992. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Mediflex Intl. Filter by specialty or product code using the sidebar.

Mediflex Intl. 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 - Mediflex Intl.

9 devices

1-9 of 9

Cleared Feb 11, 1992

PRIMARY DRESSING TRAY

K915140 · LYY

General Hospital · 90d

Cleared May 15, 1990

HEMODIALYSIS TRANSDUCER PROTECTOR

K900841 · FIB

Gastroenterology & Urology · 82d

Cleared May 24, 1989

MEDIVERSE PARENTERAL NUTRITION BAG

K891077 · KPE

General Hospital · 84d

Cleared Dec 08, 1988

BLOOD TUBING SET

K884243 · FJK

Gastroenterology & Urology · 58d

Cleared Sep 23, 1986

MEDIFLEX TRANSDUCER PROTECTOR

K863496 · FIB

Gastroenterology & Urology · 14d

Cleared Jan 24, 1986

MEDIFLEX INJECTION CAP

K855039 · GCE

General & Plastic Surgery · 38d

Cleared Nov 18, 1985

MEDIFLEX DISPOSABLE TUBING CLAMP

K854346 · FPA

General Hospital · 20d

Cleared Jun 07, 1985

I.V. ADMINISTRATION SET

K852106 · FPA

General Hospital · 23d

Cleared Oct 04, 1984

MEDIFLEX DRAINAGE BAG

K843126 · KNX

Gastroenterology & Urology · 55d

Mediflex Intl. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Mediflex Intl.

Filters