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NEUROMETRIX BIOAMPLIFIER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083322
510(k) Type
Traditional
Applicant
NEUROMETRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2009
Days to Decision
196 days
Submission Type
Summary

NEUROMETRIX BIOAMPLIFIER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083322
510(k) Type
Traditional
Applicant
NEUROMETRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2009
Days to Decision
196 days
Submission Type
Summary