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ACCU-LEAD

Page Type
Cleared 510(K)
510(k) Number
K050443
510(k) Type
Traditional
Applicant
KENTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2005
Days to Decision
192 days
Submission Type
Summary

ACCU-LEAD

Page Type
Cleared 510(K)
510(k) Number
K050443
510(k) Type
Traditional
Applicant
KENTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2005
Days to Decision
192 days
Submission Type
Summary