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AMBU SPUR (SINGLE PATIENT USE RESUSCITATOR) INFANT

Page Type
Cleared 510(K)
510(k) Number
K902261
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1990
Days to Decision
56 days

AMBU SPUR (SINGLE PATIENT USE RESUSCITATOR) INFANT

Page Type
Cleared 510(K)
510(k) Number
K902261
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1990
Days to Decision
56 days