Last synced on 30 September 2022 at 11:05 pm

ISCALERT SENSOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071165
510(k) Type
Traditional
Applicant
ALERTIS MEDICAL AS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2007
Days to Decision
195 days
Submission Type
Summary

ISCALERT SENSOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071165
510(k) Type
Traditional
Applicant
ALERTIS MEDICAL AS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2007
Days to Decision
195 days
Submission Type
Summary