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ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT

Page Type
Cleared 510(K)
510(k) Number
K970878
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1997
Days to Decision
57 days
Submission Type
Summary

ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT

Page Type
Cleared 510(K)
510(k) Number
K970878
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1997
Days to Decision
57 days
Submission Type
Summary