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HITACHI VERSIFLEX

Page Type
Cleared 510(K)
510(k) Number
K991231
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/1999
Days to Decision
42 days
Submission Type
Summary

HITACHI VERSIFLEX

Page Type
Cleared 510(K)
510(k) Number
K991231
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/1999
Days to Decision
42 days
Submission Type
Summary