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MODIFIED SINGLE PATIENT USE DISP MAN RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K903443
510(k) Type
Traditional
Applicant
PURITAN BENNETT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
17 days

MODIFIED SINGLE PATIENT USE DISP MAN RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K903443
510(k) Type
Traditional
Applicant
PURITAN BENNETT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
17 days