Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Oximeter

K-Number: K173045 · 2018-06-05

Decision Date2018-06-05
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Oximeter is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Greatmade Tech Limited. It received FDA 510(k) clearance on 2018-06-05 under 510(k) 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. 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.