Last synced on 14 November 2025 at 11:06 pm

AMBU SILICONE RESUSCITATOR INFAN/CHILD W/OPEN RESO

Page Type
Cleared 510(K)
510(k) Number
K924216
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/1992
Days to Decision
43 days
Submission Type
Statement

AMBU SILICONE RESUSCITATOR INFAN/CHILD W/OPEN RESO

Page Type
Cleared 510(K)
510(k) Number
K924216
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/1992
Days to Decision
43 days
Submission Type
Statement