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LAURUS NEEDLE CORE BIOPSY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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