Last synced on 2 December 2022 at 11:04 pm

AMBU SPUR II. ADULT SINGLE PATIENT RESUSCITATOR

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