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FDA 510(k) Application Details - K955708
Device Classification Name
System, Digital Image Communications, Radiological
More FDA Info for this Device
510(K) Number
K955708
Device Name
System, Digital Image Communications, Radiological
Applicant
COMPUMED, INC.
2245 FRANKLIN AVE.
MEETEETSE, WY 82433 US
Other 510(k) Applications for this Company
Regulation Number
892.2020
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Classification Product Code
LMD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/14/1995
Decision Date
03/01/1996
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
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