Trav-Ler Kit

FDA 510(k) K943942 · John O. Butler Co.

Unknown

510(k) numberK943942

Submission

Device name
Trav-Ler Kit
Applicant
John O. Butler Co.
Chicago, IL, US
Received
August 12, 1994
Decision date
March 8, 1995
Decision
Unknown (SESK)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JEQ – Toothbrush, Powered
Device class
Class I (low risk)
Regulation
21 CFR 872.6865
Specialty
Dental

Other 510(k)s with product code JEQ

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K200881Oral-B iO Test Drive Power Brush Trial Program KitJEQ · Traditional The Procter & Gamble Company08/27/2020SE
K141018Oral-B Test Drive Power Brush Trial Program Kit, Oral-B Test Drive Power Toothbrush Kit…JEQ · Traditional Procter & Gamble Co.09/15/2014SE
K061351Oral-B Sonic CompleteJEQ · Traditional Braun GmbH06/05/2006SE
K061199Oral B Professionalcare Series, Oral B Advancepower SeriesJEQ · Traditional Braun GmbH05/31/2006SE
K040416Sonicare Advance Toothbrush, Model 4900JEQ · Traditional Philips Oral Healthcare, Inc.07/02/2004SE
K022900Butler Gum Vari-Clean Power ToothbrushesJEQ · Traditional John O. Butler Co.11/14/2002SE
K012914Sonicwave Sonic Plaque RemoverJEQ · Traditional Homedics, Inc.10/01/2001SE
K970381Powered ToothbrushJEQ · Traditional Emjoi Action USA, Ltd.04/18/1997SE
K945248Hukuba Hyg Electric Ionic ToothbrushJEQ · Traditional Hukuba Dental Corp.01/26/1995SE
K944084Jeneric/Pentron P0WERED ToothbrustJEQ · Traditional Jeneric/Pentron, Inc.12/20/1994SE

More from Jeneric/Pentron, Inc.

510(k)DeviceDecision
K022900Butler Gum Vari-Clean Power ToothbrushesJEQ · Traditional 11/14/2002SE
K974761Butler Antibacterial Interdental ToothbrushEFW · Traditional 06/16/1998SE
K952091Vutler G.U.M. with FluorideJES · Traditional 06/28/1995SE
K950993Butler G.U.M. Antibacterial ToothbrushEFW · Traditional 06/02/1995SE
K874194Protect Drops/Same AS K874070EJK · Traditional 12/16/1987SE

Questions and answers

When was Trav-Ler Kit cleared by the FDA?

Trav-Ler Kit (K943942) received a 510(k) decision of Unknown on March 8, 1995, 208 days after the submission was received.

What is the product code of K943942?

The FDA product code is JEQ – Toothbrush, Powered, a Class I (low risk) device regulated under 21 CFR 872.6865.