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MODIFICATION TO ACCUFUSER, ACCUFUSER PLUS STANDARD PROCEDURE KIT

Page Type
Cleared 510(K)
510(k) Number
K050770
510(k) Type
Traditional
Applicant
MCKINLEY MEDICAL LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2005
Days to Decision
20 days
Submission Type
Summary

MODIFICATION TO ACCUFUSER, ACCUFUSER PLUS STANDARD PROCEDURE KIT

Page Type
Cleared 510(K)
510(k) Number
K050770
510(k) Type
Traditional
Applicant
MCKINLEY MEDICAL LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2005
Days to Decision
20 days
Submission Type
Summary