Last synced on 14 June 2024 at 11:05 pm

ASCEND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140333
510(k) Type
Traditional
Applicant
NEUROMETRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2014
Days to Decision
143 days
Submission Type
Summary

ASCEND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140333
510(k) Type
Traditional
Applicant
NEUROMETRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2014
Days to Decision
143 days
Submission Type
Summary