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BARD BIOPSY NEEDLE GUIDANCE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K883374
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1988
Days to Decision
51 days

BARD BIOPSY NEEDLE GUIDANCE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K883374
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1988
Days to Decision
51 days