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NEOPOP INFANT RESUSCITATOR WITH FLOW METER

Page Type
Cleared 510(K)
510(k) Number
K102649
510(k) Type
Traditional
Applicant
NEOFORCE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2011
Days to Decision
114 days
Submission Type
Summary

NEOPOP INFANT RESUSCITATOR WITH FLOW METER

Page Type
Cleared 510(K)
510(k) Number
K102649
510(k) Type
Traditional
Applicant
NEOFORCE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2011
Days to Decision
114 days
Submission Type
Summary