Kavo Everest Zs-Blank Models, 42, 20, and 60
FDA 510(k) K032081 · Kavo America
510(k) numberK032081
Submission
- Device name
- Kavo Everest Zs-Blank Models, 42, 20, and 60
- Applicant
- Kavo America
Deer Field, IL, US - Received
- July 7, 2003
- Decision date
- July 24, 2003
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
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| K030146 | Kavo Key Laser 1242 and Kavo Key Laser 1243+NVK · Traditional | 08/03/2005SE |
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| K050744 | Kavo Ergocom/ErgocamLLZ · Traditional | 04/21/2005SE |
| K050019 | In Exam Intraoral Dental X-Ray SystemEHD · Traditional | 01/31/2005SE |
| K042872 | Rondoflex Plus 360KOJ · Special | 11/23/2004SE |
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Questions and answers
When was Kavo Everest Zs-Blank Models, 42, 20, and 60 cleared by the FDA?
Kavo Everest Zs-Blank Models, 42, 20, and 60 (K032081) received a 510(k) decision of Substantially Equivalent on July 24, 2003, 17 days after the submission was received.
What is the product code of K032081?
The FDA product code is EIH – Powder, Porcelain, a Class II (moderate risk) device regulated under 21 CFR 872.6660.