FDA 510(k) Applications Submitted by DAKO DIAGNOSTICS LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K962037 05/24/1996 IMAGEN RESPIRATORY SCREEN DAKO DIAGNOSTICS LTD.
K973954 10/09/1997 IMAGEN RESPIRATORY SCREEN DAKO DIAGNOSTICS LTD.
K940564 02/03/1994 IDEIA(TM) CHLAMYDIA BLOCKING REAGENTS, MODIFICATION DAKO DIAGNOSTICS LTD.
K981226 03/24/1998 IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST TYPES 1,2 AND 3 DAKO DIAGNOSTICS LTD.


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