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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