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BREAST LESION LOCALIZATION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K945124
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1994
Days to Decision
34 days
Submission Type
Statement

BREAST LESION LOCALIZATION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K945124
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1994
Days to Decision
34 days
Submission Type
Statement