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REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090243
510(k) Type
Special
Applicant
Respironics Inc., Sleep & Home Respiratory Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2009
Days to Decision
95 days
Submission Type
Summary

REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090243
510(k) Type
Special
Applicant
Respironics Inc., Sleep & Home Respiratory Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2009
Days to Decision
95 days
Submission Type
Summary