Drill, Dental
FDA 510(k) K801887 · Aesculap Instruments Corp.
510(k) numberK801887
Submission
- Device name
- Drill, Dental
- Applicant
- Aesculap Instruments Corp.
Mchenry, IL, US - Received
- July 28, 1980
- Decision date
- August 20, 1980
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code DZA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K984508 | Surgical Contra-Angle Handpieces, Models 975 AE,979 E/Km, 985 Ae, 986 Ae, 988 E/Km and…DZA · Traditional | W&H Dentalwerk Buermoos GmbH | 06/25/1999SE |
| K962979 | S-53 Introral Dental SystemDZA · Traditional | Del Medical Systems Corp. | 09/25/1996SE |
| K954790 | Profile Nickel Titanium Rotary InstrumentsDZA · Traditional | Tulsa Dental Products, Ltd. | 01/16/1996SE |
| K914724 | Ada Shank ExtensionDZA · Traditional | Implant Corp. of America | 07/27/1993SE |
| K905418 | Gates Glidden DrillsDZA · Traditional | The Hygenic Corp. | 07/25/1991SE |
| K901097 | Fillock ReamerDZA · Traditional | Ivoclar North America, Inc. | 04/25/1990SE |
| K896149 | Anest-Eze Dental Drill RA#2DZA · Traditional | Signature One Products, Inc. | 01/19/1990SE |
| K884187 | Indentec Drill Ra #1DZA · Traditional | Phillip C. Crawford, D.D.S. | 12/22/1988SE |
| K811113 | Riess-LuhrDZA · Traditional | Allomedic | 06/16/1981SE |
| K801888 | Handpiece, DentalDZA · Traditional | Aesculap Instruments Corp. | 08/20/1980SE |
More from Aesculap Instruments Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K890182 | Protegraft DV 1500, 1900 & Low Por, Unigraft DVDSY · Traditional | 02/28/1990SE |
| K885046 | Insitucat Valve StripperDWQ · Traditional | 02/28/1990SE |
| K890443 | Caspar Scalp Clip, ApplierHBO · Traditional | 06/15/1989SE |
| K893121 | Robotrac (TM) Retractor ArmGAD · Traditional | 06/01/1989SE |
| K884057 | Elan-E Disposable DrapeKKX · Traditional | 10/19/1988SE |
| K880704 | Cerullo Suction RegulatorGCX · Traditional | 03/29/1988SE |
| K860016 | Aesculap Bone MillLYS · Traditional | 03/19/1986SE |
| K801888 | Handpiece, DentalDZA · Traditional | 08/20/1980SE |
| K801886 | Burr, DentalEJL · Traditional | 08/20/1980SE |
| K792558 | Container SystemFLE · Traditional | 12/27/1979SE |
Questions and answers
When was Drill, Dental cleared by the FDA?
Drill, Dental (K801887) received a 510(k) decision of Substantially Equivalent on August 20, 1980, 23 days after the submission was received.
What is the product code of K801887?
The FDA product code is DZA – Drill, Dental, Intraoral, a Class I (low risk) device regulated under 21 CFR 872.4130.