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NEURO-PATCH

Page Type
Cleared 510(K)
510(k) Number
K960470
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1996
Days to Decision
99 days
Submission Type
Summary

NEURO-PATCH

Page Type
Cleared 510(K)
510(k) Number
K960470
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1996
Days to Decision
99 days
Submission Type
Summary