Orange Medical Instruments, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Orange Medical Instruments, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1982 to 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Orange Medical Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orange Medical Instruments, Inc.
12 devices
Cleared
Mar 13, 1986
CONTINUCATH
Anesthesiology
9d
Cleared
Oct 03, 1985
BETA SCAN TRENDS METER
Chemistry
160d
Cleared
Dec 18, 1984
MICRO-BETA U100 SYRINGE
General Hospital
7d
Cleared
Nov 05, 1984
TRENDS LANCET
General Hospital
34d
Cleared
Aug 23, 1984
BETA SCAN DRYSTIX
Chemistry
142d
Cleared
May 09, 1984
BETAJECT BD U100
General Hospital
204d
Cleared
Apr 05, 1984
CLICK-COUNT U100 INSULIN SYRINGE
General Hospital
170d
Cleared
Nov 14, 1983
BETA SCAN REAGENT STRIP
Hematology
96d
Cleared
Sep 26, 1983
NEOCATH 1000 W/HEPCOTE
Anesthesiology
38d
Cleared
Aug 12, 1983
BETA I PROGRAMMABLE INFUSION PUMP
General Hospital
59d
Cleared
Jul 19, 1983
BETA SCAN NORMAL CONTROL SOLUTION
Chemistry
68d
Cleared
Oct 26, 1982
DISPOSABLE MICRO-INFUSION SYSTEM
Microbiology
22d