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BREAST LOCALIZATION NEEDLES

Page Type
Cleared 510(K)
510(k) Number
K881730
510(k) Type
Traditional
Applicant
HART ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/1988
Days to Decision
21 days

BREAST LOCALIZATION NEEDLES

Page Type
Cleared 510(K)
510(k) Number
K881730
510(k) Type
Traditional
Applicant
HART ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/1988
Days to Decision
21 days