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RESPCARE HYBRID AV MASK

Page Type
Cleared 510(K)
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)
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