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CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090646
510(k) Type
Traditional
Applicant
CHEST M.I., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2009
Days to Decision
134 days
Submission Type
Summary

CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090646
510(k) Type
Traditional
Applicant
CHEST M.I., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2009
Days to Decision
134 days
Submission Type
Summary