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FDA 510(k) Application Details - K980918
Device Classification Name
System, Digital Image Communications, Radiological
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510(K) Number
K980918
Device Name
System, Digital Image Communications, Radiological
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
595 MINER RD.
CLEVELAND, OH 44143 US
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Contact
ROBERT L TUROCY
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Regulation Number
892.2020
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Classification Product Code
LMD
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More FDA Info for this Product Code
Date Received
03/11/1998
Decision Date
06/03/1998
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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