FDA 510(k) Application Details - K993665

Device Classification Name System, X-Ray, Stationary

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510(K) Number K993665
Device Name System, X-Ray, Stationary
Applicant GE MEDICAL SYSTEMS, INC.
P.O. BOX 414
MILWAUKEE, WI 53201 US
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Contact LARRY A KROGER
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Regulation Number 892.1680

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Classification Product Code KPR
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Date Received 10/29/1999
Decision Date 11/12/1999
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 Y
Expedited Review



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