Ortho Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ortho Instruments - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Ortho Instruments has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1978 to 1980. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Ortho Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ortho Instruments
6 devices
Cleared
Dec 31, 1980
ORTHO HEMATOLOGY CONTROL
Hematology
26d
Cleared
Dec 31, 1980
ORTHO HEMOTOLOGY CONTROL-NORMAL
Hematology
26d
Cleared
Dec 31, 1980
ORTHO HEMATOLOGY CONTROL ABNORMAL LOW
Hematology
26d
Cleared
Oct 10, 1980
ORTHO SPECTRUM
Hematology
38d
Cleared
Sep 09, 1980
ORTHO AUTOMATED CELL COUNTER
Hematology
64d
Cleared
Sep 14, 1978
HEMAC LASER HEMATOLOGY SYSTEM
Hematology
66d