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MODIFIED SINGLE PATIENT USE DISP MAN RESUSCITATOR

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