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Orion Corp.

21 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
RUBALEX, MODIFICATION (K912391)Orion Corp.1992-05-04
RESUBMITTED MODIFIED RUBALEX (K901637)Orion Corp.1990-04-26
RESUBMITTED SCANORA (K884650)Orion Corp.1989-03-16
DENTOCULT SM-STRIP MUTANS (K890199)Orion Corp.1989-03-02
MAMEX DC MAG MG12 (K881506)Orion Corp.1988-06-10
MAMEX DC MG11 (K881505)Orion Corp.1988-06-10
MAMEX DC S SL10/MG14 (K874040)Orion Corp.1987-11-23
MODIFIED CHLAMYSET ANTIGEN (K872744)Orion Corp.1987-09-22
CHLAMYSET ANTIBODY EIA (K864457)Orion Corp.1987-09-11
DENTOCULT-SM CULTURE-PADDLE (K872301)Orion Corp.1987-09-11
ORICULT-N CULTURE-PADDLE (K872058)Orion Corp.1987-06-10
IMMUNOCHEMICAL ASSAY OF APOLIPOPROTEIN A1 (K861883)Orion Corp.1986-10-29
IMMUNOCHEMICAL ASSAY APOLIPOPROTEIN B (K861882)Orion Corp.1986-10-29
MYOLEX (K863730)Orion Corp.1986-10-15
MICROALBUMINURIA ASSAY (K862671)Orion Corp.1986-09-18
IMMUNOCHEMICAL ASSAY OF C-REACTIVE PROTEIN (K860679)Orion Corp.1986-08-04
RUBALEX (REVISED VERSION) (K861881)Orion Corp.1986-06-04
CHLAMYSET ANTIGEN (K853401)Orion Corp.1986-04-28
RUBALEX (K852788)Orion Corp.1986-03-12
ROTALEX (K860529)Orion Corp.1986-03-04
DENTOCULT CULTURE-PADDLE (K851164)Orion Corp.1985-10-29

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