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FDA 510(k)

LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS

K-Number: K094046 · 2010-05-14

Decision Date2010-05-14
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS is the device name listed in this FDA 510(k) record. The listed applicant is Masimo Corporation. It received FDA 510(k) clearance on 2010-05-14 under 510(k) number K094046. 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 LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS?

LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS is a medical device that received FDA 510(k) clearance on 2010-05-14. The listed applicant is Masimo Corporation. The 510(k) number is K094046.

When did LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS receive FDA 510(k) clearance?

LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS received FDA 510(k) clearance on 2010-05-14, under 510(k) number K094046.

Who is the listed applicant for LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS?

The FDA 510(k) record lists Masimo Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS?

The FDA product code for LNCS OXIMETRY SENSORS, REPROCESSED LNCS OXIMETRY SENSORS 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 Masimo 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.

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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.

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