MASIMO LNOP/LNCS/M-LNCS MULTISITE-L OXIMETRY SENSORS
K-Number: K111888 · 2011-09-23
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Device Summary
Frequently Asked Questions
What is the MASIMO LNOP/LNCS/M-LNCS MULTISITE-L OXIMETRY SENSORS?
MASIMO LNOP/LNCS/M-LNCS MULTISITE-L OXIMETRY SENSORS is a medical device that received FDA 510(k) clearance on 2011-09-23. The listed applicant is Masimo Corporation. The 510(k) number is K111888.
When did MASIMO LNOP/LNCS/M-LNCS MULTISITE-L OXIMETRY SENSORS receive FDA 510(k) clearance?
MASIMO LNOP/LNCS/M-LNCS MULTISITE-L OXIMETRY SENSORS received FDA 510(k) clearance on 2011-09-23, under 510(k) number K111888.
Who is the listed applicant for MASIMO LNOP/LNCS/M-LNCS MULTISITE-L 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 MASIMO LNOP/LNCS/M-LNCS MULTISITE-L OXIMETRY SENSORS?
The FDA product code for MASIMO LNOP/LNCS/M-LNCS MULTISITE-L 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.
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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