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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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