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ORTHO 8000

Page Type
Cleared 510(K)
510(k) Number
K963186
510(k) Type
Traditional
Applicant
INNER VISION MRI LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1996
Days to Decision
90 days
Submission Type
Summary

ORTHO 8000

Page Type
Cleared 510(K)
510(k) Number
K963186
510(k) Type
Traditional
Applicant
INNER VISION MRI LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1996
Days to Decision
90 days
Submission Type
Summary