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NEOPIP PATIENT CIRCUIT WITH PEEP

Page Type
Cleared 510(K)
510(k) Number
K103833
510(k) Type
Traditional
Applicant
NEOFORCE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2011
Days to Decision
111 days
Submission Type
Summary

NEOPIP PATIENT CIRCUIT WITH PEEP

Page Type
Cleared 510(K)
510(k) Number
K103833
510(k) Type
Traditional
Applicant
NEOFORCE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2011
Days to Decision
111 days
Submission Type
Summary