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MODIFIED SINGLE PATIENT USE DISP. MANUAL RESUSCIT.

Page Type
Cleared 510(K)
510(k) Number
K911971
510(k) Type
Traditional
Applicant
PURITAN BENNETT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1991
Days to Decision
98 days
Submission Type
Statement

MODIFIED SINGLE PATIENT USE DISP. MANUAL RESUSCIT.

Page Type
Cleared 510(K)
510(k) Number
K911971
510(k) Type
Traditional
Applicant
PURITAN BENNETT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1991
Days to Decision
98 days
Submission Type
Statement