LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD
K-Number: K180583 · 2018-06-28
Device Summary
Frequently Asked Questions
What is the LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD?
LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD is a medical device that received FDA 510(k) clearance on 2018-06-28. The listed applicant is Richard Wolf Medical Instruments Corporation. The 510(k) number is K180583.
When did LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD receive FDA 510(k) clearance?
LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD received FDA 510(k) clearance on 2018-06-28, under 510(k) number K180583.
Who is the listed applicant for LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD?
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 LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD?
The FDA product code for LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD 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.