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NEUROVISION SE (NERVEANA)

Page Type
Cleared 510(K)
510(k) Number
K102862
510(k) Type
Traditional
Applicant
NEUROVISION MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2010
Days to Decision
82 days
Submission Type
Summary

NEUROVISION SE (NERVEANA)

Page Type
Cleared 510(K)
510(k) Number
K102862
510(k) Type
Traditional
Applicant
NEUROVISION MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2010
Days to Decision
82 days
Submission Type
Summary