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FDA 510(k)

M-LNCS OXIMETRY SENSORS, REPROCESSED M-LNCS OXIMETRY SENSORS

K-Number: K110723 · 2011-07-28

ApplicantMasimo Corporation
Decision Date2011-07-28
Product CodeNLF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

M-LNCS OXIMETRY SENSORS, REPROCESSED M-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 2011-07-28 under 510(k) number K110723. The device is classified under product code NLF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M-LNCS OXIMETRY SENSORS, REPROCESSED M-LNCS OXIMETRY SENSORS?

M-LNCS OXIMETRY SENSORS, REPROCESSED M-LNCS OXIMETRY SENSORS is a medical device that received FDA 510(k) clearance on 2011-07-28. The listed applicant is Masimo Corporation. The 510(k) number is K110723.

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

M-LNCS OXIMETRY SENSORS, REPROCESSED M-LNCS OXIMETRY SENSORS received FDA 510(k) clearance on 2011-07-28, under 510(k) number K110723.

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

The FDA product code for M-LNCS OXIMETRY SENSORS, REPROCESSED M-LNCS OXIMETRY SENSORS is NLF.

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Related Devices (Code: NLF)

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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.

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