FDA 510(k) Application Details - K233080

Device Classification Name System, X-Ray, Tomography, Computed

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510(K) Number K233080
Device Name System, X-Ray, Tomography, Computed
Applicant Nano-X AI Ltd.
Shefayim Commercial Center, PO Box 25
Shefayim 6099000 IL
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Contact Neta Sherman
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Regulation Number 892.1750

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Classification Product Code JAK
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Date Received 09/26/2023
Decision Date 02/08/2024
Decision SESE - SUBST EQUIV
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K233080


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