D Camera Controller
K-Number: K211332 · 2021-10-01
Decision Date2021-10-01
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
D Camera Controller is a medical device manufactured by Richard Wolf Medical Instruments Corporation. It received FDA 510(k) clearance on 2021-10-01 under approval number K211332. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the D Camera Controller?
D Camera Controller is a medical device that received FDA 510(k) clearance on 2021-10-01. It is manufactured by Richard Wolf Medical Instruments Corporation. The 510(k) number is K211332.
When was D Camera Controller approved by the FDA?
D Camera Controller received FDA 510(k) clearance on 2021-10-01, under approval number K211332.
What company makes D Camera Controller?
D Camera Controller is manufactured by Richard Wolf Medical Instruments Corporation.
What is the FDA product code for D Camera Controller?
The FDA product code for D Camera Controller is FET.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.