Last synced on 2 May 2025 at 11:05 pm

NEUTROLUMENPN SYSTEM, MODEL 1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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