Vip Victor Interactive Probe

FDA 510(k) K960245 · Pro-Dentec

Substantially Equivalent

510(k) numberK960245

Submission

Device name
Vip Victor Interactive Probe
Applicant
Pro-Dentec
Chicago, IL, US
Received
January 16, 1996
Decision date
April 4, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EIX – Probe, Periodontic
Device class
Class I (low risk)
Regulation
21 CFR 872.4565
Specialty
Dental

Other 510(k)s with product code EIX

510(k)DeviceApplicantDecision
K944848The Vivacare T.P.S. ProbeEIX · Traditional Rms Div.12/14/1994SE
K936221Probe Tip/Peri Probe/Peri Probe Comp.EIX · Traditional Pd International AB08/01/1994SE
K890333Albumin ReagentEIX · Traditional Alpkem Corp.02/17/1989SE
K880827Accutek Periodontal ProbeEIX · Traditional Sweet Micro Systems, Inc.04/12/1988SE
K875076Florida ProbeEIX · Traditional Florida Probe Corp.03/10/1988SE
K870280Accudent AccuprobeEIX · Traditional Accudent, Inc.06/08/1987SE
K871504Disposable Periodontal ProbeEIX · Traditional Periodontal Health Brush, Inc.05/06/1987SE
K823324Dental Instruments - ProbesEIX · Traditional Miltex, Inc.11/24/1982SE

More from Miltex, Inc.

510(k)DeviceDecision
K880589Rota-Dent Tooth CleanerJEQ · Traditional 05/11/1988SE

Questions and answers

When was Vip Victor Interactive Probe cleared by the FDA?

Vip Victor Interactive Probe (K960245) received a 510(k) decision of Substantially Equivalent on April 4, 1996, 79 days after the submission was received.

What is the product code of K960245?

The FDA product code is EIX – Probe, Periodontic, a Class I (low risk) device regulated under 21 CFR 872.4565.