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AESCULAP ANGLED NEUROENDOSCOPES

Page Type
Cleared 510(K)
510(k) Number
K964281
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1997
Days to Decision
175 days
Submission Type
Summary

AESCULAP ANGLED NEUROENDOSCOPES

Page Type
Cleared 510(K)
510(k) Number
K964281
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1997
Days to Decision
175 days
Submission Type
Summary