Medical Device Manufacturer · US , Mchenry , IL

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

22 submissions · 22 cleared · Since 1977

Total

Cleared

Denied

Med Fusion Systems, Inc. has 22 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 22 cleared submissions from 1977 to 1987. Primary specialty: General Hospital.

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

Med Fusion Systems, 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 Fusion Systems, Inc.

22 devices

1-12 of 22

Cleared Dec 29, 1987

INFUMED 300 AMBULATORY INFUSION PUMP

K873961 · FRN

General Hospital · 91d

Cleared May 06, 1987

AMBULATORY INFUSION PUMP DRUG RESERVOIR

K870524 · FRN

General Hospital · 89d

Cleared Apr 09, 1987

INTRODUCER, PERCUTANEOUS

General Hospital · 71d

Cleared Oct 14, 1986

BAG SPIKE EXTENSION SET

K863814 · FPA

General Hospital · 14d

Cleared Jun 02, 1986

VOLUME CONTROL SET WITH EXTENSION

K860616 · FPA

General Hospital · 103d

Cleared Apr 09, 1986

IV FILTER EXTENSION SET

K860803 · FPB

General Hospital · 36d

Cleared Jan 22, 1985

INFUSET W/HUBER NEEDLE

K844313 · FMI

General Hospital · 77d

Cleared Oct 16, 1984

EXTENSION SET W/INJECTION SITE

K842984 · FPA

General Hospital · 78d

Cleared Jul 20, 1984

BENT WINGED MINI-VOL INFUSION SET

K842143 · FPA

General Hospital · 51d

Cleared Jun 05, 1984

THREE WAY INFUSION SET

K841882 · FPA

General Hospital · 29d

Cleared Mar 14, 1978

TOILET SAFETY RAIL

K772275 · LDQ

General & Plastic Surgery · 95d

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

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

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