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ROTEX SCREW BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K854404
510(k) Type
Traditional
Applicant
MEADOX SURGIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1985
Days to Decision
31 days

ROTEX SCREW BIOPSY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K854404
510(k) Type
Traditional
Applicant
MEADOX SURGIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1985
Days to Decision
31 days