FDA 510(k) Application Details - K230491

Device Classification Name Laparoscope, General & Plastic Surgery

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510(K) Number K230491
Device Name Laparoscope, General & Plastic Surgery
Applicant Human Xtensions Ltd.
Meir Ariel 4
Netanya 4250574 IL
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Contact Hani Rauch
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Regulation Number 876.1500

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Classification Product Code GCJ
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Date Received 02/23/2023
Decision Date 05/10/2023
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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