Oximeter
K-Number: K173045 · 2018-06-05
ApplicantShenzhen Greatmade Tech Limited
Decision Date2018-06-05
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Oximeter is a medical device manufactured by Shenzhen Greatmade Tech Limited. It received FDA 510(k) clearance on 2018-06-05 under approval number K173045. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Oximeter?
Oximeter is a medical device that received FDA 510(k) clearance on 2018-06-05. It is manufactured by Shenzhen Greatmade Tech Limited. The 510(k) number is K173045.
When was Oximeter approved by the FDA?
Oximeter received FDA 510(k) clearance on 2018-06-05, under approval number K173045.
What company makes Oximeter?
Oximeter is manufactured by Shenzhen Greatmade Tech Limited.
What is the FDA product code for Oximeter?
The FDA product code for Oximeter is DQA.
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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.