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FDA 510(k) Applications Submitted by NEUSOFT POSITRON MEDICAL SYSTEMS CO., LTD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090178
01/26/2009
ATTRIUS, MODEL PET150A6001, ATTRIUS L, MODEL PET150A8001, TRUESIGHT, MODEL NSP-P6C, TRUESIGHT, MODEL NSP-P8
NEUSOFT POSITRON MEDICAL SYSTEMS CO., LTD
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