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AMBU SINGLE PATIENT USE PEEP VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923976
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1993
Days to Decision
151 days
Submission Type
Statement

AMBU SINGLE PATIENT USE PEEP VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923976
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1993
Days to Decision
151 days
Submission Type
Statement