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FDA 510(k) Applications Submitted by TZONG-FUH KUO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042556
09/20/2004
SHINEBALL PVC MANUAL RESUSCIATOR, ENT-1001, ENT-1003, ENT-1005, SHINEBALL SILICONE MANUAL RESUSCIATOR, ENT-1022,
ENTER MEDICAL CORPORATION
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