Columbia Bioscience, Inc.
Columbia Bioscience, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 1999.
Top product codes for Columbia Bioscience, Inc.
Recent clearances by Columbia Bioscience, Inc.
- K990462 — IS H. PYLORI IGG ELISA TEST SYSTEM
- K991274 — MUMPS IGG ELISA TEST SYSTEM
- K984228 — IS ANTI-TPO IGG ELISA TEST SYSTEM
- K983605 — IS BORRELIA BURGDORFERI IGG/IGM ELISA TEST SYSTEM
- K983606 — IS BORRELIA BURGDORFERI IGM TEST SYSTEM
- K983553 — ANTI-TG IGG ELISA TEST SYSTEM
- K982348 — EBNA-1 IGM ELISA TEST SYSTEM
- K982350 — EA-D IGM ELISA TEST SYSTEM
- K982352 — VCA IGM ELISA TEST SYSTEM
- K983390 — IS-ANTI-MPO IGG ELISA TEST SYSTEM
- K983740 — IS-ANTI-PR3 IGG ELISA TEST SYSTEM
- K962113 — ANTHOS PHACTS VERSION MICROPLATE READER
- K961183 — CBI 7520 READER
Data sourced from openFDA. This site is unofficial and independent of the FDA.