Medical Device Manufacturer · FI , 20101 Turku

Orion Corp. - FDA 510(k) Cleared Devices

21 submissions · 20 cleared · Since 1985

Total

Cleared

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.

FDA 510(k) Regulatory Record - Orion Corp.

21 devices

1-12 of 21

Cleared May 04, 1992

RUBALEX, MODIFICATION

K912391 · LQN

Microbiology · 346d

Cleared Apr 26, 1990

RESUBMITTED MODIFIED RUBALEX

DENTOCULT SM-STRIP MUTANS

MODIFIED CHLAMYSET ANTIGEN

K872744 · LJP

Microbiology · 74d

Cleared Sep 11, 1987

CHLAMYSET ANTIBODY EIA

K864457 · LJC

Microbiology · 303d

Cleared Sep 11, 1987

DENTOCULT-SM CULTURE-PADDLE

K872301 · JSI

Microbiology · 88d

Cleared Jun 10, 1987

ORICULT-N CULTURE-PADDLE

K872058 · JSI

Microbiology · 13d

Cleared Oct 29, 1986

IMMUNOCHEMICAL ASSAY APOLIPOPROTEIN B

K861882 · MSJ

Immunology · 167d

Orion Corp. - FDA 510(k) Cleared Devices

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