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SMARTSCREENER-PLUS2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090579
510(k) Type
Traditional
Applicant
Intelligent Hearing Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2009
Days to Decision
126 days
Submission Type
Summary

SMARTSCREENER-PLUS2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090579
510(k) Type
Traditional
Applicant
Intelligent Hearing Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2009
Days to Decision
126 days
Submission Type
Summary