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AMBU SPUR II. ADULT SINGLE PATIENT RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K042682
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2004
Days to Decision
47 days
Submission Type
Statement

AMBU SPUR II. ADULT SINGLE PATIENT RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K042682
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2004
Days to Decision
47 days
Submission Type
Statement