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SINGLE USE MANUAL RESUSCITATOR PEEP VALVE

Page Type
Cleared 510(K)
510(k) Number
K932799
510(k) Type
Traditional
Applicant
ENGINEERED MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1993
Days to Decision
86 days
Submission Type
Statement

SINGLE USE MANUAL RESUSCITATOR PEEP VALVE

Page Type
Cleared 510(K)
510(k) Number
K932799
510(k) Type
Traditional
Applicant
ENGINEERED MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1993
Days to Decision
86 days
Submission Type
Statement