Degucast 40
FDA 510(k) K922790 · Degussa AG
510(k) numberK922790
Submission
- Device name
- Degucast 40
- Applicant
- Degussa AG
South Plainfield, NJ, US - Received
- June 9, 1992
- Decision date
- December 3, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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Questions and answers
When was Degucast 40 cleared by the FDA?
Degucast 40 (K922790) received a 510(k) decision of Substantially Equivalent on December 3, 1992, 177 days after the submission was received.
What is the product code of K922790?
The FDA product code is EJH – Alloy, Metal, Base, a Class II (moderate risk) device regulated under 21 CFR 872.3710.