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FDA 510(k) Applications Submitted by TAKESHI OZAKI
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040870
04/02/2004
SHIMADZU IMAGE AMPLIFIER, MODEL IA-16L/HS
SHIMADZU CORP.
K031771
06/09/2003
SHIMADZU COLLIMATOR R-30H
SHIMADZU CORP.
K041763
06/30/2004
SHIMADZU MOBILE X-RAY SYSTEM MUX-100D SERIES
SHIMADZU CORP.
K032443
08/08/2003
DIGITAL ANGIOGRAPHY SYSTEM DIGITEX SAFIRE
SHIMADZU CORP.
K033184
10/01/2003
LATERAL ANGIOGRAPHIC C-ARM SUPPORT MH-400
SHIMADZU CORP.
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