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BREATHEX OMEGA CPAP DEVICE, MODEL 322

Page Type
Cleared 510(K)
510(k) Number
K052597
510(k) Type
Traditional
Applicant
HOFFMAN LABORATORIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2005
Days to Decision
86 days
Submission Type
Summary

BREATHEX OMEGA CPAP DEVICE, MODEL 322

Page Type
Cleared 510(K)
510(k) Number
K052597
510(k) Type
Traditional
Applicant
HOFFMAN LABORATORIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2005
Days to Decision
86 days
Submission Type
Summary