FDA 510(k) Applications Submitted by MICRON CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K991239 04/12/1999 VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2 MICRON CORP.
K032995 09/25/2003 SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL) MICRON CORP.
K133170 10/17/2013 QUICK JET M MICRON CORP.


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