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LUTZ NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K013892
510(k) Type
Traditional
Applicant
BALLARD MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2002
Days to Decision
230 days
Submission Type
Summary

LUTZ NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K013892
510(k) Type
Traditional
Applicant
BALLARD MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2002
Days to Decision
230 days
Submission Type
Summary