Medical Device Manufacturer · US , Mchenry , IL

Organon Teknika Corp. - FDA 510(k) Cleared Devices

130 submissions · 129 cleared · Since 1980

Recent clearances: BACT/ALERT CSR, MDA D-DIMER, BACT/ALERT MB CULTURE BOTTLE

130

Total

129

Cleared

Denied

Organon Teknika Corp. has 129 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 129 cleared submissions from 1980 to 2000.

Browse the FDA 510(k) cleared devices submitted by Organon Teknika Corp. Filter by specialty or product code using the sidebar.

Organon Teknika Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Organon Teknika Corp.

130 devices

1-12 of 130

1 2 3 4

BACT/ALERT MB CULTURE BOTTLE

BACT/ALERT MP PROCESS BOTTLE

1 2 3 4

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Organon Teknika Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Organon Teknika Corp.

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