Dental Instruments - Probes
FDA 510(k) K823324 · Miltex, Inc.
510(k) numberK823324
Submission
- Device name
- Dental Instruments - Probes
- Applicant
- Miltex, Inc.
Walker, MI, US - Received
- November 8, 1982
- Decision date
- November 24, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code EIX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K960245 | Vip Victor Interactive ProbeEIX · Traditional | Pro-Dentec | 04/04/1996SE |
| K944848 | The Vivacare T.P.S. ProbeEIX · Traditional | Rms Div. | 12/14/1994SE |
| K936221 | Probe Tip/Peri Probe/Peri Probe Comp.EIX · Traditional | Pd International AB | 08/01/1994SE |
| K890333 | Albumin ReagentEIX · Traditional | Alpkem Corp. | 02/17/1989SE |
| K880827 | Accutek Periodontal ProbeEIX · Traditional | Sweet Micro Systems, Inc. | 04/12/1988SE |
| K875076 | Florida ProbeEIX · Traditional | Florida Probe Corp. | 03/10/1988SE |
| K870280 | Accudent AccuprobeEIX · Traditional | Accudent, Inc. | 06/08/1987SE |
| K871504 | Disposable Periodontal ProbeEIX · Traditional | Periodontal Health Brush, Inc. | 05/06/1987SE |
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| K092855 | Miltex Membrane Tack KitDZL · Traditional | 12/29/2009SE |
| K083796 | Miltex Aspirating Syringe, Miltex Petite Aspirating Syringe, Miltex Self-Aspirating…EJI · Traditional | 03/09/2009SE |
| K072563 | Miltex Rigid Container SystemsKCT · Traditional | 02/12/2008SE |
| K061033 | Miltex Rigid Sterilization Container System, (47 Components)KCT · Traditional | 12/12/2006SE |
| K052018 | Miltex Ligating ClipFZP · Traditional | 11/04/2005SE |
| K050570 | Miltex Rigid Sterilization Container SystemKCT · Traditional | 07/25/2005SE |
| K043013 | Miltex Laparoscopic InstrumentsHET · Traditional | 03/04/2005SE |
| K013888 | Fixation (Steinmann) PinsHTY · Traditional | 05/01/2002SE |
| K954185 | Re-Bag Multi-Use Pouch, Large & SmallKCT · Traditional | 12/04/1995SESK |
Questions and answers
When was Dental Instruments - Probes cleared by the FDA?
Dental Instruments - Probes (K823324) received a 510(k) decision of Substantially Equivalent on November 24, 1982, 16 days after the submission was received.
What is the product code of K823324?
The FDA product code is EIX – Probe, Periodontic, a Class I (low risk) device regulated under 21 CFR 872.4565.