D Camera Controller
K-Number: K211332 · 2021-10-01
Device Summary
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. The listed applicant is Richard Wolf Medical Instruments Corporation. The 510(k) number is K211332.
When did D Camera Controller receive FDA 510(k) clearance?
D Camera Controller received FDA 510(k) clearance on 2021-10-01, under 510(k) number K211332.
Who is the listed applicant for D Camera Controller?
The FDA 510(k) record lists Richard Wolf Medical Instruments Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for D Camera Controller?
The FDA product code for D Camera Controller is FET.
Other records listing Richard Wolf Medical Instruments Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FET)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.