ReCross
K-Number: K210431 · 2021-07-15
Device Summary
Frequently Asked Questions
What is the ReCross?
ReCross is a medical device that received FDA 510(k) clearance on 2021-07-15. The listed applicant is Imds Operations B.V.. The 510(k) number is K210431.
When did ReCross receive FDA 510(k) clearance?
ReCross received FDA 510(k) clearance on 2021-07-15, under 510(k) number K210431.
Who is the listed applicant for ReCross?
The FDA 510(k) record lists Imds Operations B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ReCross?
The FDA product code for ReCross is DQY.
Other records listing Imds Operations B.V. 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: DQY)
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.