FDA 510(k) Applications Submitted by Aurolab

FDA 510(k) Number Submission Date Device Name Applicant
K221759 06/17/2022 Cornisol Aurolab
K140039 01/07/2014 POLYCRYL AUROLAB
K024090 12/11/2002 NYLON SUTURE AUROLAB
K024091 12/11/2002 SILK SUTURES AUROLAB


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