Last synced on 14 November 2025 at 11:06 pm

INTRACAVITY NEEDLE GUIDE KIT

Page Type
Cleared 510(K)
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)
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