Last synced on 14 November 2025 at 11:06 pm

LAURUS NEEDLE CORE BIOPSY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K960317
510(k) Type
Traditional
Applicant
LAURUS MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1996
Days to Decision
52 days
Submission Type
Statement

LAURUS NEEDLE CORE BIOPSY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K960317
510(k) Type
Traditional
Applicant
LAURUS MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1996
Days to Decision
52 days
Submission Type
Statement