Interplak Home Plaque Removal Instrument
FDA 510(k) K935561 · Bausch & Lomb, Inc.
510(k) numberK935561
Submission
- Device name
- Interplak Home Plaque Removal Instrument
- Applicant
- Bausch & Lomb, Inc.
Tucker, GA, US - Received
- November 17, 1993
- Decision date
- January 26, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Other 510(k)s with product code JEQ
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|---|---|---|---|
| K200881 | Oral-B iO Test Drive Power Brush Trial Program KitJEQ · Traditional | The Procter & Gamble Company | 08/27/2020SE |
| K141018 | Oral-B Test Drive Power Brush Trial Program Kit, Oral-B Test Drive Power Toothbrush Kit…JEQ · Traditional | Procter & Gamble Co. | 09/15/2014SE |
| K061351 | Oral-B Sonic CompleteJEQ · Traditional | Braun GmbH | 06/05/2006SE |
| K061199 | Oral B Professionalcare Series, Oral B Advancepower SeriesJEQ · Traditional | Braun GmbH | 05/31/2006SE |
| K040416 | Sonicare Advance Toothbrush, Model 4900JEQ · Traditional | Philips Oral Healthcare, Inc. | 07/02/2004SE |
| K022900 | Butler Gum Vari-Clean Power ToothbrushesJEQ · Traditional | John O. Butler Co. | 11/14/2002SE |
| K012914 | Sonicwave Sonic Plaque RemoverJEQ · Traditional | Homedics, Inc. | 10/01/2001SE |
| K970381 | Powered ToothbrushJEQ · Traditional | Emjoi Action USA, Ltd. | 04/18/1997SE |
| K943942 | Trav-Ler KitJEQ · Traditional | John O. Butler Co. | 03/08/1995SESK |
| K945248 | Hukuba Hyg Electric Ionic ToothbrushJEQ · Traditional | Hukuba Dental Corp. | 01/26/1995SE |
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| K210975 | Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for PresbyopiaLPL · Traditional | 05/24/2021SE |
| K200416 | Boston One Step Liquid Enzymatic CleanerMRC · Traditional | 09/23/2020SE |
| K192005 | Bausch + Lomb PreVue Inserter for enVista PreloadedMSS · Special | 10/04/2019SE |
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Questions and answers
When was Interplak Home Plaque Removal Instrument cleared by the FDA?
Interplak Home Plaque Removal Instrument (K935561) received a 510(k) decision of Substantially Equivalent on January 26, 1994, 70 days after the submission was received.
What is the product code of K935561?
The FDA product code is JEQ – Toothbrush, Powered, a Class I (low risk) device regulated under 21 CFR 872.6865.