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DIGITAL ANGIOGRAPHY SYSTEM DIGITEX SAFIRE

Page Type
Cleared 510(K)
510(k) Number
K032443
510(k) Type
Abbreviated
Applicant
SHIMADZU CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2004
Days to Decision
196 days
Submission Type
Statement

DIGITAL ANGIOGRAPHY SYSTEM DIGITEX SAFIRE

Page Type
Cleared 510(K)
510(k) Number
K032443
510(k) Type
Abbreviated
Applicant
SHIMADZU CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2004
Days to Decision
196 days
Submission Type
Statement