FDA 510(k) Application Details - K233906

Device Classification Name Recorder, Magnetic Tape, Medical

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510(K) Number K233906
Device Name Recorder, Magnetic Tape, Medical
Applicant Wellysis Corp.
8F, 425 Teheran-ro, Gangnam-gu
Seoul 06159 KR
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Contact Sam Engelman
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Regulation Number 870.2800

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Classification Product Code DSH
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Date Received 12/12/2023
Decision Date 02/16/2024
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review

FDA Source Information for K233906


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