Last synced on 14 November 2025 at 11:06 pm

ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KIT, ACCUFUSER INFUSION KIT

Page Type
Cleared 510(K)
510(k) Number
K023098
510(k) Type
Traditional
Applicant
MCKINLEY INFUSER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2002
Days to Decision
82 days
Submission Type
Summary

ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KIT, ACCUFUSER INFUSION KIT

Page Type
Cleared 510(K)
510(k) Number
K023098
510(k) Type
Traditional
Applicant
MCKINLEY INFUSER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2002
Days to Decision
82 days
Submission Type
Summary