Orion Corp.

21 FDA 510(k) medical device clearances.

Top product codes for Orion Corp.

Recent clearances by Orion Corp.

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.