Instrument,Filling,Plastic,Dental
FDA 510(k) K945077 · Worldwide Dental, Inc.
510(k) numberK945077
Submission
- Device name
- Instrument,Filling,Plastic,Dental
- Applicant
- Worldwide Dental, Inc.
Clearwater, FL, US - Received
- October 17, 1994
- Decision date
- November 30, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Other 510(k)s with product code EKJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K961714 | Aseptylum, Uni-CarrierEKJ · Traditional | Distriflor S.A. | 06/10/1996SE |
| K953707 | Medtrol Dental KitEKJ · Traditional | Medtrol, Inc. | 01/04/1996SE |
| K945815 | Dental KitEKJ · Traditional | Constancy Ent., Inc. | 07/19/1995SE |
| K951607 | Sureflex FilesEKJ · Traditional | Dentsply Intl. | 06/22/1995SE |
| K943820 | Stat PakEKJ · Traditional | Magnum Instruments, Inc. | 11/02/1994SE |
| K943351 | Maunal Disposable Dental InstrumentsEKJ · Traditional | Magnum Instruments, Inc. | 10/07/1994SE |
| K943584 | Presterilized Endodontic FilesEKJ · Traditional | Dentsply Intl. | 09/21/1994SE |
| K935127 | Southland Sterile Dental SystemEKJ · Traditional | Southland, Ltd. | 07/28/1994SE |
| K941954 | Non-Fogging Dental MirrorEKJ · Traditional | Buffalo Dental Mfg. Co., Inc. | 07/08/1994SE |
| K925115 | Amd Dentist and Hygienist KitsEKJ · Traditional | Advance Medical Designs, Inc. | 07/05/1994SE |
More from Advance Medical Designs, Inc.
Questions and answers
When was Instrument,Filling,Plastic,Dental cleared by the FDA?
Instrument,Filling,Plastic,Dental (K945077) received a 510(k) decision of Substantially Equivalent on November 30, 1994, 44 days after the submission was received.
What is the product code of K945077?
The FDA product code is EKJ – Burnisher, Operative, a Class I (low risk) device regulated under 21 CFR 872.4565.