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BIPAP DUET LX BI-LEVEL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000994
510(k) Type
Special
Applicant
Respironics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2000
Days to Decision
86 days
Submission Type
Summary

BIPAP DUET LX BI-LEVEL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000994
510(k) Type
Special
Applicant
Respironics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2000
Days to Decision
86 days
Submission Type
Summary