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NEOPIP INFANT RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K072021
510(k) Type
Traditional
Applicant
NEOFORCE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2007
Days to Decision
51 days
Submission Type
Summary

NEOPIP INFANT RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K072021
510(k) Type
Traditional
Applicant
NEOFORCE GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2007
Days to Decision
51 days
Submission Type
Summary