Orion Corp. - FDA 510(k) Cleared Devices
21
Total
20
Cleared
0
Denied
Orion Corp. has 20 FDA 510(k) cleared medical devices. Based in 20101 Turku, FI.
Historical record: 20 cleared submissions from 1985 to 1992. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Orion Corp. Filter by specialty or product code using the sidebar.
21 devices
Cleared
May 04, 1992
RUBALEX, MODIFICATION
Microbiology
346d
Cleared
Apr 26, 1990
RESUBMITTED MODIFIED RUBALEX
Microbiology
17d
Cleared
Mar 16, 1989
RESUBMITTED SCANORA
Radiology
129d
Cleared
Mar 02, 1989
DENTOCULT SM-STRIP MUTANS
Microbiology
43d
Cleared
Jun 10, 1988
MAMEX DC MG11
Radiology
60d
Cleared
Jun 10, 1988
MAMEX DC MAG MG12
Radiology
60d
Cleared
Nov 23, 1987
MAMEX DC S SL10/MG14
Radiology
49d
Cleared
Sep 22, 1987
MODIFIED CHLAMYSET ANTIGEN
Microbiology
74d
Cleared
Sep 11, 1987
CHLAMYSET ANTIBODY EIA
Microbiology
303d
Cleared
Sep 11, 1987
DENTOCULT-SM CULTURE-PADDLE
Microbiology
88d
Cleared
Jun 10, 1987
ORICULT-N CULTURE-PADDLE
Microbiology
13d
Cleared
Oct 29, 1986
IMMUNOCHEMICAL ASSAY APOLIPOPROTEIN B
Immunology
167d
Cleared
Oct 29, 1986
IMMUNOCHEMICAL ASSAY OF APOLIPOPROTEIN A1
Immunology
167d
Cleared
Oct 15, 1986
MYOLEX
Immunology
22d
Cleared
Sep 18, 1986
MICROALBUMINURIA ASSAY
Immunology
66d
Cleared
Aug 04, 1986
IMMUNOCHEMICAL ASSAY OF C-REACTIVE PROTEIN
Immunology
160d
Cleared
Jun 04, 1986
RUBALEX (REVISED VERSION)
Microbiology
27d
Cleared
Apr 28, 1986
CHLAMYSET ANTIGEN
Microbiology
259d
Cleared
Mar 12, 1986
RUBALEX
Microbiology
254d
Cleared
Mar 04, 1986
ROTALEX
Microbiology
21d
Cleared
Oct 29, 1985
DENTOCULT CULTURE-PADDLE
Microbiology
221d