MODIFICATION TO LNCS OXIMETRY SENSORS
K-Number: K051212 · 2005-07-12
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO LNCS OXIMETRY SENSORS?
MODIFICATION TO LNCS OXIMETRY SENSORS is a medical device that received FDA 510(k) clearance on 2005-07-12. The listed applicant is Masimo Corporation. The 510(k) number is K051212.
When did MODIFICATION TO LNCS OXIMETRY SENSORS receive FDA 510(k) clearance?
MODIFICATION TO LNCS OXIMETRY SENSORS received FDA 510(k) clearance on 2005-07-12, under 510(k) number K051212.
Who is the listed applicant for MODIFICATION TO 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 MODIFICATION TO LNCS OXIMETRY SENSORS?
The FDA product code for MODIFICATION TO 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.
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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