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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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