EasyOne Filter
K-Number: K221250 · 2022-11-22
Device Summary
Frequently Asked Questions
What is the EasyOne Filter?
EasyOne Filter is a medical device that received FDA 510(k) clearance on 2022-11-22. The listed applicant is Ndd Medizintechnik AG. The 510(k) number is K221250.
When did EasyOne Filter receive FDA 510(k) clearance?
EasyOne Filter received FDA 510(k) clearance on 2022-11-22, under 510(k) number K221250.
Who is the listed applicant for EasyOne Filter?
The FDA 510(k) record lists Ndd Medizintechnik AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EasyOne Filter?
The FDA product code for EasyOne Filter is CAH.
Other records listing Ndd Medizintechnik AG 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: CAH)
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.