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GENERAL (BIOPSY) NEEDLE GUIDE KIT, STERILE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892071
510(k) Type
Traditional
Applicant
AMEDIC USA
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
8/8/1989
Days to Decision
130 days

GENERAL (BIOPSY) NEEDLE GUIDE KIT, STERILE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892071
510(k) Type
Traditional
Applicant
AMEDIC USA
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
8/8/1989
Days to Decision
130 days