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RESPCARE HYBRID AV MASK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062224
510(k) Type
Special
Applicant
RESPCARE INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2006
Days to Decision
15 days
Submission Type
Summary

RESPCARE HYBRID AV MASK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062224
510(k) Type
Special
Applicant
RESPCARE INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2006
Days to Decision
15 days
Submission Type
Summary