Last synced on 1 March 2024 at 11:05 pm

HICP200 Patient/Monitor Interconnect Cable

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161010
510(k) Type
Traditional
Applicant
InnerSpace Neuro Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2016
Days to Decision
192 days
Submission Type
Summary

HICP200 Patient/Monitor Interconnect Cable

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161010
510(k) Type
Traditional
Applicant
InnerSpace Neuro Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2016
Days to Decision
192 days
Submission Type
Summary