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ENDOVIEW SPPHIRE LENS SET

Page Type
Cleared 510(K)
510(k) Number
K971853
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/1997
Days to Decision
78 days
Submission Type
Summary

ENDOVIEW SPPHIRE LENS SET

Page Type
Cleared 510(K)
510(k) Number
K971853
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/1997
Days to Decision
78 days
Submission Type
Summary