FDA 510(k) Application Details - K240146

Device Classification Name System, Imaging, Pulsed Echo, Ultrasonic

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510(K) Number K240146
Device Name System, Imaging, Pulsed Echo, Ultrasonic
Applicant Bard Access Systems, Inc.
605 N 5600 W
Salt Lake City, UT 84116 US
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Contact Samira Saeed
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Regulation Number 892.1560

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Classification Product Code IYO
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Date Received 01/19/2024
Decision Date 02/18/2024
Decision SESE - SUBST EQUIV
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review

FDA Source Information for K240146


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