Orion Diagnostica, Div. Orion Corp. is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.
Orion Diagnostica, Div. Orion Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Orion Diagnostica, Div. Orion Corp. has 4 FDA 510(k) cleared medical devices. Based in 02101 Espoo, FI.
Historical record: 4 cleared submissions from 1995 to 2003. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Orion Diagnostica, Div. Orion Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orion Diagnostica, Div. Orion Corp.
4 devices
Cleared
Oct 10, 2003
ORION DIAGNOSTICA QUIKREAD CRP KIT AND QUIKREAD CRP CONTROL
Immunology
141d
Cleared
Dec 03, 2002
ORION DIAGNOSTICA ULTRASENSITIVE CRP KIT, MODEL 68025, & ORION DIAGNOSTICA...
Immunology
153d
Cleared
Jun 27, 1997
PYLORISET EIA-G (68926)
Microbiology
60d
Cleared
Apr 05, 1995
PYLORISET DRY
Microbiology
289d