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VACUUM ASSISTED CORE BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K010400
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2001
Days to Decision
162 days
Submission Type
Statement

VACUUM ASSISTED CORE BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K010400
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2001
Days to Decision
162 days
Submission Type
Statement