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FDA 510(k) Applications Submitted by Kelley Breheim
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120612
02/29/2012
MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT
MEDTRONIC INC.
K212077
07/02/2021
Teleflex Rusch SoftSimplastic Foley Catheters
Teleflex Medical, Inc.
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