MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D
K-Number: K100617 · 2010-05-28
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Device Summary
Frequently Asked Questions
What is the MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D?
MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D is a medical device that received FDA 510(k) clearance on 2010-05-28. The listed applicant is Masimo Corporation. The 510(k) number is K100617.
When did MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D receive FDA 510(k) clearance?
MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D received FDA 510(k) clearance on 2010-05-28, under 510(k) number K100617.
Who is the listed applicant for MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D?
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 RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D?
The FDA product code for MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D 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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