ALOKA ARIETTA 850
K-Number: K173739 · 2018-02-28
Device Summary
Frequently Asked Questions
What is the ALOKA ARIETTA 850?
ALOKA ARIETTA 850 is a medical device that received FDA 510(k) clearance on 2018-02-28. The listed applicant is Hitachi Healthcare Americas Corporation. The 510(k) number is K173739.
When did ALOKA ARIETTA 850 receive FDA 510(k) clearance?
ALOKA ARIETTA 850 received FDA 510(k) clearance on 2018-02-28, under 510(k) number K173739.
Who is the listed applicant for ALOKA ARIETTA 850?
The FDA 510(k) record lists Hitachi Healthcare Americas Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALOKA ARIETTA 850?
The FDA product code for ALOKA ARIETTA 850 is IYN.
Other records listing Hitachi Healthcare Americas 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: IYN)
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.