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OPART (INCLUDING OPART ULTRA AND ULTRA GRADIENT UPGRADE KIT)

Page Type
Cleared 510(K)
510(k) Number
K023207
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2002
Days to Decision
14 days
Submission Type
Summary

OPART (INCLUDING OPART ULTRA AND ULTRA GRADIENT UPGRADE KIT)

Page Type
Cleared 510(K)
510(k) Number
K023207
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2002
Days to Decision
14 days
Submission Type
Summary