FDA 510(k) Applications Submitted by BIOLIFE, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K130324 02/08/2013 STATSEAL DISC BIOLIFE, LLC
K080210 01/28/2008 PRO QR ADVANCED FORMULA POWDER BIOLIFE, LLC
K070520 02/23/2007 PRO QR (QUICK RELIEF) POWDER (FOR MINOR EXTERNAL BLEEDING FROM WOUNDS & PROCEDURES) BIOLIFE, LLC


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