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SENOCOR 360 CIRCUMFERENTIAL VACUUM ASSISTED BIOPSY DEVICE, 8 GAUGE

Page Type
Cleared 510(K)
510(k) Number
K023923
510(k) Type
Special
Applicant
SENORX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2002
Days to Decision
16 days
Submission Type
Statement

SENOCOR 360 CIRCUMFERENTIAL VACUUM ASSISTED BIOPSY DEVICE, 8 GAUGE

Page Type
Cleared 510(K)
510(k) Number
K023923
510(k) Type
Special
Applicant
SENORX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2002
Days to Decision
16 days
Submission Type
Statement