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MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K890665
510(k) Type
Traditional
Applicant
DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1989
Days to Decision
267 days

MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K890665
510(k) Type
Traditional
Applicant
DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1989
Days to Decision
267 days