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MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K990379
510(k) Type
Special
Applicant
DEXIDE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1999
Days to Decision
24 days
Submission Type
Summary

MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K990379
510(k) Type
Special
Applicant
DEXIDE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1999
Days to Decision
24 days
Submission Type
Summary