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INTRACAVITY NEEDLE GUIDE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955668
510(k) Type
Traditional
Applicant
ARLANDA MEDICINSKA INSTRUMENT CO. AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
7/30/1997
Days to Decision
595 days
Submission Type
Statement

INTRACAVITY NEEDLE GUIDE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955668
510(k) Type
Traditional
Applicant
ARLANDA MEDICINSKA INSTRUMENT CO. AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
7/30/1997
Days to Decision
595 days
Submission Type
Statement