FDA 510(k) Applications Submitted by Judith Ogden

FDA 510(k) Number Submission Date Device Name Applicant
K100304 02/03/2010 ST AIA PACK HBA1C Tosoh BioScience, Inc.
K111335 05/12/2011 ST AIA-PACK ACTH, AND ST AIA-PACK ACTH CALIBRATOR SET MODEL 025221 AND 025321 Tosoh BioScience, Inc.
K111762 06/23/2011 ST AIA-PACK DHEA-S CALIBRATOR SET Tosoh BioScience, Inc.
K093960 12/23/2009 ST AIA-PACK CYSTATIN C, MODEL 025217 Tosoh BioScience, Inc.


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