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AMBU NEONATE SILICONE RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K993278
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2000
Days to Decision
230 days
Submission Type
Statement

AMBU NEONATE SILICONE RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K993278
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2000
Days to Decision
230 days
Submission Type
Statement