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BIERMAN BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K841299
510(k) Type
Traditional
Applicant
POPPER & SONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1984
Days to Decision
33 days

BIERMAN BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K841299
510(k) Type
Traditional
Applicant
POPPER & SONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1984
Days to Decision
33 days