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FDA 510(k) Applications Submitted by MICHIGAN INSTRUMENTS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K073079
10/31/2007
THUMPER, MODEL: 1008
MICHIGAN INSTRUMENTS, INC.
K962237
06/11/1996
THUMPER CARDIOPULMONARY RESUSCITATOR
MICHIGAN INSTRUMENTS, INC.
K972525
07/07/1997
THUMPER
MICHIGAN INSTRUMENTS, INC.
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