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AMNISCREEN HOME DETECTION LINER KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071100
510(k) Type
Traditional
Applicant
COMMON SENSE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2007
Days to Decision
179 days
Submission Type
Summary

AMNISCREEN HOME DETECTION LINER KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071100
510(k) Type
Traditional
Applicant
COMMON SENSE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2007
Days to Decision
179 days
Submission Type
Summary