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KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K900903
510(k) Type
Traditional
Applicant
MILEX PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/1990
Days to Decision
65 days

KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K900903
510(k) Type
Traditional
Applicant
MILEX PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/1990
Days to Decision
65 days