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AMBU SINGLE PATIENT USE PEEP VALVE

Page Type
Cleared 510(K)
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)
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