Last synced on 13 May 2022 at 11:05 pm

Ambu SPUR II Adult Resuscitator, Ambu SPUR II Pediatric Resuscitator, Ambu SPUR II Infant Resuscitator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152931
510(k) Type
Abbreviated
Applicant
AMBU A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
8/29/2016
Days to Decision
329 days
Submission Type
Summary

Ambu SPUR II Adult Resuscitator, Ambu SPUR II Pediatric Resuscitator, Ambu SPUR II Infant Resuscitator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152931
510(k) Type
Abbreviated
Applicant
AMBU A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
8/29/2016
Days to Decision
329 days
Submission Type
Summary