CMDR 2C (Multiple Models)
K-Number: K201575 · 2020-07-08
Device Summary
Frequently Asked Questions
What is the CMDR 2C (Multiple Models)?
CMDR 2C (Multiple Models) is a medical device that received FDA 510(k) clearance on 2020-07-08. The listed applicant is Minxray, Inc.. The 510(k) number is K201575.
When did CMDR 2C (Multiple Models) receive FDA 510(k) clearance?
CMDR 2C (Multiple Models) received FDA 510(k) clearance on 2020-07-08, under 510(k) number K201575.
Who is the listed applicant for CMDR 2C (Multiple Models)?
The FDA 510(k) record lists Minxray, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CMDR 2C (Multiple Models)?
The FDA product code for CMDR 2C (Multiple Models) is IZL.
Other records listing Minxray, Inc. 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: IZL)
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.