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BREAST LESION LOCALIZATION NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924270
510(k) Type
Traditional
Applicant
CORE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1992
Days to Decision
30 days
Submission Type
Statement

BREAST LESION LOCALIZATION NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924270
510(k) Type
Traditional
Applicant
CORE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1992
Days to Decision
30 days
Submission Type
Statement