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NEUROCATH AG

Page Type
Cleared 510(K)
510(k) Number
K081942
510(k) Type
Special
Applicant
VYGON NEURO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2008
Days to Decision
35 days
Submission Type
Summary

NEUROCATH AG

Page Type
Cleared 510(K)
510(k) Number
K081942
510(k) Type
Special
Applicant
VYGON NEURO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2008
Days to Decision
35 days
Submission Type
Summary