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FDA 510(k) Applications Submitted by Anita J. Nemeth
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180801
03/28/2018
Actreen Hi-Lite Cath, Actreen Hi-Lite Set
B. Braun Medical Inc.
K192577
09/19/2019
Actreen Hi-Lite Intermittent Urinary Catheters
B. Braun Medical Inc.
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