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AMBU SPUR (SINGLE PATIENT USE RESUSCITATOR)

Page Type
Cleared 510(K)
510(k) Number
K883434
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1988
Days to Decision
30 days

AMBU SPUR (SINGLE PATIENT USE RESUSCITATOR)

Page Type
Cleared 510(K)
510(k) Number
K883434
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1988
Days to Decision
30 days