FDA 510(k) Applications Submitted by Kericure Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K131384 05/14/2013 KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE KERICURE INC.
K212521 08/10/2021 Field Shield Wound Dressing Kericure Inc.


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