Oximeter
K-Number: K173045 · 2018-06-05
Device Summary
Frequently Asked Questions
What is the Oximeter?
Oximeter is a medical device that received FDA 510(k) clearance on 2018-06-05. The listed applicant is Shenzhen Greatmade Tech Limited. The 510(k) number is K173045.
When did Oximeter receive FDA 510(k) clearance?
Oximeter received FDA 510(k) clearance on 2018-06-05, under 510(k) number K173045.
Who is the listed applicant for Oximeter?
The FDA 510(k) record lists Shenzhen Greatmade Tech Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Oximeter?
The FDA product code for Oximeter is DQA.
Related Devices (Code: DQA)
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.