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MINIVIDAS INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K923579
510(k) Type
Traditional
Applicant
BIOMERIEUX VITEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
207 days
Submission Type
Summary

MINIVIDAS INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K923579
510(k) Type
Traditional
Applicant
BIOMERIEUX VITEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
207 days
Submission Type
Summary