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MODIFIED INTRAVENOUS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K896813
510(k) Type
Traditional
Applicant
SAFEGUARD NEEDLE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1990
Days to Decision
319 days

MODIFIED INTRAVENOUS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K896813
510(k) Type
Traditional
Applicant
SAFEGUARD NEEDLE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1990
Days to Decision
319 days