Medical Device Manufacturer · US , Mchenry , IL

Future Impex Corp. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1983

Total

Cleared

Denied

Future Impex Corp. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1983 to 1986. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Future Impex Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Future Impex Corp.

14 devices

1-12 of 14

ERMA HB-METER MODEL 303N

K854687 · KHG

Hematology · 196d

Cleared Apr 04, 1986

DIGITAL-9 KEY LEUCOCYTE COUNTER

K854685 · GKM

Hematology · 135d

Cleared Feb 24, 1986

ERMA PC-604 BLOOD CELL COUNTER

K854677 · GKL

Hematology · 96d

Cleared Feb 24, 1986

ERMA PC-602 PC-603 BLOOD CELL COUNTER

K854678 · GKL

Hematology · 81d

Cleared Feb 20, 1986

PHOTIC-100 SPECTROPHOTOMETER

K854679 · JJQ

Chemistry · 92d

Cleared Nov 20, 1984

MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT

K843934 · DPS

Cardiovascular · 42d

Cleared Oct 24, 1984

ST-200A W/MAXIMAL VOLUNTARY VENTILLAT-

FUKUNDA SANGYO UNITS ELECTRONIC SPIRO

K832430 · BZG

Anesthesiology · 69d

Cleared Sep 29, 1983

FUKUNDA SANGYA UNITS PULMOTESTER PM60

K832431 · BZG

Anesthesiology · 69d

Future Impex Corp. - FDA 510(k) Cleared Devices

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