Cordis Ventricular Antechamber (Va)
FDA 510(k) K955832 · Cordis Corp.
510(k) numberK955832
Submission
- Device name
- Cordis Ventricular Antechamber (Va)
- Applicant
- Cordis Corp.
Miami Lakes, FL, US - Received
- December 26, 1995
- Decision date
- March 25, 1996
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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Questions and answers
When was Cordis Ventricular Antechamber (Va) cleared by the FDA?
Cordis Ventricular Antechamber (Va) (K955832) received a 510(k) decision of Substantially Equivalent on March 25, 1996, 90 days after the submission was received.
What is the product code of K955832?
The FDA product code is JXG – Shunt, Central Nervous System And Components, a Class II (moderate risk) device regulated under 21 CFR 882.5550.