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FDA 510(k) Application Details - K992506
Device Classification Name
More FDA Info for this Device
510(K) Number
K992506
Device Name
MINI 6800 DIGITAL MOBILE C-ARM
Applicant
GE DEC MEDICAL SYSTEMS
384 WRIGHT BROTHERS DR.
SALT LAKE CITY, UT 84116 US
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Contact
TED L PARROT
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Regulation Number
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Classification Product Code
OXO
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Date Received
07/27/1999
Decision Date
08/19/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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