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CATHETER INSERTION KIT

Page Type
Cleared 510(K)
510(k) Number
K833432
510(k) Type
Traditional
Applicant
CLINIPAD CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/1983
Days to Decision
84 days

CATHETER INSERTION KIT

Page Type
Cleared 510(K)
510(k) Number
K833432
510(k) Type
Traditional
Applicant
CLINIPAD CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/1983
Days to Decision
84 days