The Nellcor pulse oximetry monitor interface cable
K-Number: K172482 · 2017-12-15
Device Summary
Frequently Asked Questions
What is the The Nellcor pulse oximetry monitor interface cable?
The Nellcor pulse oximetry monitor interface cable is a medical device that received FDA 510(k) clearance on 2017-12-15. The listed applicant is Covidien. The 510(k) number is K172482.
When did The Nellcor pulse oximetry monitor interface cable receive FDA 510(k) clearance?
The Nellcor pulse oximetry monitor interface cable received FDA 510(k) clearance on 2017-12-15, under 510(k) number K172482.
Who is the listed applicant for The Nellcor pulse oximetry monitor interface cable?
The FDA 510(k) record lists Covidien as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for The Nellcor pulse oximetry monitor interface cable?
The FDA product code for The Nellcor pulse oximetry monitor interface cable is DQA.
Related Clinical Trials
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.
Other records listing Covidien 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: 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.