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CORE BIOPSY NEEDLE, CATALOG CODE #54006

Page Type
Cleared 510(K)
510(k) Number
K891537
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1989
Days to Decision
32 days

CORE BIOPSY NEEDLE, CATALOG CODE #54006

Page Type
Cleared 510(K)
510(k) Number
K891537
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1989
Days to Decision
32 days