MASIMO SET REUSABLE OXIMETRY SENSORS
K-Number: K113596 · 2012-02-24
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Device Summary
Frequently Asked Questions
What is the MASIMO SET REUSABLE OXIMETRY SENSORS?
MASIMO SET REUSABLE OXIMETRY SENSORS is a medical device that received FDA 510(k) clearance on 2012-02-24. The listed applicant is Masimo Corporation. The 510(k) number is K113596.
When did MASIMO SET REUSABLE OXIMETRY SENSORS receive FDA 510(k) clearance?
MASIMO SET REUSABLE OXIMETRY SENSORS received FDA 510(k) clearance on 2012-02-24, under 510(k) number K113596.
Who is the listed applicant for MASIMO SET REUSABLE 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 SET REUSABLE OXIMETRY SENSORS?
The FDA product code for MASIMO SET REUSABLE 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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