FDA 510(k) Application Details - K243273

Device Classification Name Pump, Infusion, Insulin Bolus

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510(K) Number K243273
Device Name Pump, Infusion, Insulin Bolus
Applicant CeQur SA
Ebenaustrasse 10
Horw Luzern 6048 CH
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Contact Michael Simpson
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Regulation Number 880.5725

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Classification Product Code OPP
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Date Received 10/16/2024
Decision Date 11/13/2024
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee CH - Clinical Chemistry
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review

FDA Source Information for K243273


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