Nyquist.IQ
K-Number: K212890 · 2021-12-13
Device Summary
Frequently Asked Questions
What is the Nyquist.IQ?
Nyquist.IQ is a medical device that received FDA 510(k) clearance on 2021-12-13. The listed applicant is Omega Medical Imaging, LLC. The 510(k) number is K212890.
When did Nyquist.IQ receive FDA 510(k) clearance?
Nyquist.IQ received FDA 510(k) clearance on 2021-12-13, under 510(k) number K212890.
Who is the listed applicant for Nyquist.IQ?
The FDA 510(k) record lists Omega Medical Imaging, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nyquist.IQ?
The FDA product code for Nyquist.IQ is JAA.
Other records listing Omega Medical Imaging, LLC 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: JAA)
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.