Last synced on 21 June 2024 at 11:04 pm

AMBU SPUR (SINGLE PATIENT USE RESUSCITATOR) INFANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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