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MODIFICATION TO ACCUFUSER, ACCUFUSER PLUS STANDARD PROCEDURE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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