LIBBE RECTAL TUBE (FORMERLY A YANKAUER SUCTION TUBE)— 510(k) K962259

Name: FDA 510(k) clearance K962259
Creator: U.S. Food and Drug Administration
Published: 1996-08-29

Substantially Equivalent

Tiller Mind Body, Inc.

FDA 510(k) clearance K962259 for LIBBE RECTAL TUBE (FORMERLY A YANKAUER SUCTION TUBE), Substantially Equivalent on 1996-08-29. Applicant: Tiller Mind Body, Inc.. Device class: 2.

Clearance details

Applicant: Tiller Mind Body, Inc.
Product code: Code KPL
Device class: Class 2
Regulation: 21 CFR 876.5220
Advisory panel: Gastroenterology, Urology
Date received: 1996-06-12
Decision date: 1996-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.