Last synced on 20 December 2024 at 11:05 pm

REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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