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NEEDLES, CANNULAS, CYSTOTOMES

Page Type
Cleared 510(K)
510(k) Number
K782169
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1979
Days to Decision
46 days

NEEDLES, CANNULAS, CYSTOTOMES

Page Type
Cleared 510(K)
510(k) Number
K782169
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1979
Days to Decision
46 days