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COAXIAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K971842
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/1997
Days to Decision
32 days
Submission Type
Summary

COAXIAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K971842
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/1997
Days to Decision
32 days
Submission Type
Summary