LINDLEY II RESUSCITATOR— 510(k) K881689

Name: FDA 510(k) clearance K881689
Creator: U.S. Food and Drug Administration
Published: 1988-07-08

Substantially Equivalent

Lindley Resuscitator, Inc.

FDA 510(k) clearance K881689 for LINDLEY II RESUSCITATOR, Substantially Equivalent on 1988-07-08. Applicant: Lindley Resuscitator, Inc.. Device class: 2.

Clearance details

Applicant: Lindley Resuscitator, Inc.
Product code: Code BYT
Device class: Class 2
Regulation: 21 CFR 868.5935
Advisory panel: Anesthesiology
Date received: 1988-04-19
Decision date: 1988-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Meridian, MS, US

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