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LINDLEY II RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K881689
510(k) Type
Traditional
Applicant
LINDLEY RESUSCITATOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1988
Days to Decision
80 days

LINDLEY II RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K881689
510(k) Type
Traditional
Applicant
LINDLEY RESUSCITATOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1988
Days to Decision
80 days