FDA 510(k) Applications Submitted by COLTENE/WHALEDENT GMBH & CO. KG

FDA 510(k) Number Submission Date Device Name Applicant
K041023 04/20/2004 STAY-PUT IMPREGNATED COLTENE/WHALEDENT GMBH & CO. KG
K032662 08/28/2003 GUTTAFLOW COLTENE/WHALEDENT GMBH & CO. KG


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