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KOO AMERICAS VALVE PEEP, MODEL KM-809

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050918
510(k) Type
Traditional
Applicant
KOO AMERICAS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2005
Days to Decision
55 days
Submission Type
Summary

KOO AMERICAS VALVE PEEP, MODEL KM-809

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050918
510(k) Type
Traditional
Applicant
KOO AMERICAS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2005
Days to Decision
55 days
Submission Type
Summary