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TROTEX II SCREW NEEDLE BIOPSY INSTR. SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792316
510(k) Type
Traditional
Applicant
URSUS KONSULT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1979
Days to Decision
32 days

TROTEX II SCREW NEEDLE BIOPSY INSTR. SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792316
510(k) Type
Traditional
Applicant
URSUS KONSULT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1979
Days to Decision
32 days