Future Impex Corp. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
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
Cleared
Jun 23, 1986
ST-90 SPIRO ANALIZER
Anesthesiology
73d
Cleared
Jun 04, 1986
TE-25 COAGURO METER
Hematology
196d
Cleared
Jun 04, 1986
ERMA HB-METER MODEL 303N
Hematology
196d
Cleared
Apr 04, 1986
DIGITAL-9 KEY LEUCOCYTE COUNTER
Hematology
135d
Cleared
Feb 24, 1986
ERMA PC-604 BLOOD CELL COUNTER
Hematology
96d
Cleared
Feb 24, 1986
ERMA PC-602 PC-603 BLOOD CELL COUNTER
Hematology
81d
Cleared
Feb 20, 1986
PHOTIC-100 SPECTROPHOTOMETER
Chemistry
92d
Cleared
Nov 20, 1984
MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT
Cardiovascular
42d
Cleared
Oct 24, 1984
ST-200A W/MAXIMAL VOLUNTARY VENTILLAT-
Cardiovascular
34d
Cleared
Oct 24, 1984
PM-80 PULMOTESTER
Anesthesiology
13d
Cleared
Sep 29, 1983
FUKUNDA SANGYO UNITS ELECTRONIC SPIRO
Anesthesiology
69d
Cleared
Sep 29, 1983
FUKUNDA SANGYA UNITS PULMOTESTER PM60
Anesthesiology
69d
Cleared
Sep 29, 1983
SPIRO ANALYZER ST-100 AUTOMATIC SPIRO
Anesthesiology
69d
Cleared
Sep 29, 1983
AUTOMATIC SPIROMETER ST-200
Anesthesiology
69d