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NEUTROLUMENPN SYSTEM, MODEL 1000

Page Type
Cleared 510(K)
510(k) Number
K082223
510(k) Type
Traditional
Applicant
NEUROLUMEN, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2009
Days to Decision
258 days
Submission Type
Statement

NEUTROLUMENPN SYSTEM, MODEL 1000

Page Type
Cleared 510(K)
510(k) Number
K082223
510(k) Type
Traditional
Applicant
NEUROLUMEN, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2009
Days to Decision
258 days
Submission Type
Statement